Pulse

JSON twin: https://www.healthaidb.com/software/pulse.json

Company Name

NuVasive

Product URL

https://www.nuvasive.com/surgical-solutions/pulse/

Company URL

https://www.nuvasive.com

Categories

• clinical Care
• administrative Operations
• patient Facing
• diagnostic Support
• surgical Care
• clinical Workflow Automation
• imaging Software
• wayfinding
• neuromonitoring
• radiation Therapy
• surgical Planning
• robotics
• software Tool
• software Development
• regulatory Compliance
• health Equity
• clinical Assessment Tools
• Clinical
• Administrative
• Diagnostic
• Surgical
• Workflow
• Imaging
• Navigation
• Radiation Reduction
• Rod Bending
• Smart Tools
• Modular Architecture
• Fda 510(k) Clearance
• Ce Mark Approval
• Global Availability
• Clinical Evaluations
• Spine Procedures

Summary

Pulse is an integrated technology platform by NuVasive designed to enhance spine surgery by combining multiple technologies into a single system, aiming to improve surgical efficiency and patient outcomes.

Description

NuVasive's Pulse platform integrates neuromonitoring, surgical planning, rod bending, radiation reduction, imaging, and navigation functions into a single system. It is designed to improve workflow, reduce surgical variability, and increase reproducibility of surgical outcomes in spine procedures. The platform supports a wide range of spine surgeries, from fusions to complex corrections, and is engineered to be utilized in 100% of spine surgeries. Pulse's modular architecture allows for flexible technology packages, enabling surgeons to select tools tailored to specific pathologies in spine surgery procedures. Additionally, Pulse's wireless functionality allows operating room staff to access technologies independently, facilitating a seamless, optimized workflow. The platform also features an extensible architecture to support future applications, including robotics and smart tools. Pulse has received FDA 510(k) clearance and CE Mark approval, indicating its compliance with regulatory standards for medical devices. It is currently available in targeted global regions, with clinical evaluations underway in multiple countries throughout Europe. The platform is designed to be utilized in 100% of spine procedures, from open to less invasive techniques, enhancing a surgeon's capabilities to make better, more informed clinical decisions for their patients.

Api Available

unknown

Certifications

• FDA 510(k) clearance
• CE mark certification

Company Founding

1997

Company Offices

• United States
• Germany
• France
• United Kingdom
• Italy
• Spain
• Netherlands
• Sweden
• Denmark
• Norway

Compliance

• HIPAA
• FDA 510(k) clearance
• CE mark certification

Customers

Data Residency

US-only

Data Standards

• HL7
• FHIR
• DICOM
• SNOMED
• ICD-10

Deployment Model

• on_prem

Features

• 2D and 3D imaging and navigation
• Integrated Global Alignment (iGA) for surgical planning
• Neuromonitoring with automatic nerve detection
• Radiation reduction through LessRay technology
• Patient-specific rod bending with Bendini technology
• Modular architecture for flexible technology packages
• Wireless connectivity for seamless team collaboration
• Compatibility with Siemens Healthineers' Cios Spin 3D mobile C-arm

Id

SW0586

Integration Partners

Integrations

• Siemens Healthineers' Cios Spin 3D mobile C-arm

Languages Supported

• English
• German
• French
• Spanish
• Italian
• Dutch
• Swedish
• Danish
• Norwegian
• Finnish
• Portuguese
• Greek
• Turkish
• Russian
• Polish
• Czech
• Hungarian
• Romanian
• Bulgarian
• Serbian
• Croatian

Last Updated

2025-10-11

License

commercial

Market Segment

• enterprise
• smb
• consumer

Optional Modules

• Spine robotics module

Os Platforms

• Windows

Pricing Details

Contact vendor for pricing information.

Pricing Model

enterprise_quote

Privacy Features

• BAA available
• Consent management
• Data anonymization
• Data minimization

Product Code

SW0586

Product Name

Pulse

Ratings

Regions Available

• United States
• Europe
• Global

Related Urls

• https://www.fda.gov/medical-devices/software-medical-device-samd/artificial-intelligence-enabled-medical-devices

Release Year

Security Features

• Data encryption at rest and in transit
• Role-based access control (RBAC)
• Audit logs
• 2FA

Specialties

• Spine Surgery
• Orthopedics
• Neurosurgery
• Minimally Invasive Surgery
• Robotic-assisted Surgery
• Surgical Planning
• Imaging
• Navigation
• Neuromonitoring
• Radiation Reduction
• Rod Bending
• Surgical Workflow
• Modular Technology
• Fda 510(k) Clearance
• Ce Mark Approval
• Global Availability
• Clinical Evaluations
• Spine Procedures
• Surgical Efficiency
• Patient Outcomes

Support Channels

System Requirements

Windows OS

Target Users

• clinicians
• surgeons
• operating room staff
• hospital administrators
• patients

Training Options

Type

product

User Reviews

Version

1.0

Alternatives

See related products

Canonical JSON

{
  "product_name": "Pulse",
  "company_name": "NuVasive",
  "product_url": "https://www.nuvasive.com/surgical-solutions/pulse/",
  "company_url": "https://www.nuvasive.com",
  "related_urls": [
    "https://www.fda.gov/medical-devices/software-medical-device-samd/artificial-intelligence-enabled-medical-devices"
  ],
  "product_code": "SW0586",
  "summary": "Pulse is an integrated technology platform by NuVasive designed to enhance spine surgery by combining multiple technologies into a single system, aiming to improve surgical efficiency and patient outcomes.",
  "description": "NuVasive's Pulse platform integrates neuromonitoring, surgical planning, rod bending, radiation reduction, imaging, and navigation functions into a single system. It is designed to improve workflow, reduce surgical variability, and increase reproducibility of surgical outcomes in spine procedures. The platform supports a wide range of spine surgeries, from fusions to complex corrections, and is engineered to be utilized in 100% of spine surgeries. Pulse's modular architecture allows for flexible technology packages, enabling surgeons to select tools tailored to specific pathologies in spine surgery procedures. Additionally, Pulse's wireless functionality allows operating room staff to access technologies independently, facilitating a seamless, optimized workflow. The platform also features an extensible architecture to support future applications, including robotics and smart tools. Pulse has received FDA 510(k) clearance and CE Mark approval, indicating its compliance with regulatory standards for medical devices. It is currently available in targeted global regions, with clinical evaluations underway in multiple countries throughout Europe. The platform is designed to be utilized in 100% of spine procedures, from open to less invasive techniques, enhancing a surgeon's capabilities to make better, more informed clinical decisions for their patients.",
  "categories": [
    "clinical Care",
    "administrative Operations",
    "patient Facing",
    "diagnostic Support",
    "surgical Care",
    "clinical Workflow Automation",
    "imaging Software",
    "wayfinding",
    "neuromonitoring",
    "radiation Therapy",
    "surgical Planning",
    "robotics",
    "software Tool",
    "software Development",
    "regulatory Compliance",
    "health Equity",
    "clinical Assessment Tools",
    "Clinical",
    "Administrative",
    "Patient-facing",
    "Diagnostic",
    "Surgical",
    "Workflow",
    "Imaging",
    "Navigation",
    "Neuromonitoring",
    "Radiation Reduction",
    "Rod Bending",
    "Surgical Planning",
    "Robotics",
    "Smart Tools",
    "Modular Architecture",
    "Fda 510(k) Clearance",
    "Ce Mark Approval",
    "Global Availability",
    "Clinical Evaluations",
    "Spine Procedures"
  ],
  "market_segment": [
    "enterprise",
    "smb",
    "consumer"
  ],
  "target_users": [
    "clinicians",
    "surgeons",
    "operating room staff",
    "hospital administrators",
    "patients"
  ],
  "specialties": [
    "Spine Surgery",
    "Orthopedics",
    "Neurosurgery",
    "Minimally Invasive Surgery",
    "Robotic-assisted Surgery",
    "Surgical Planning",
    "Imaging",
    "Navigation",
    "Neuromonitoring",
    "Radiation Reduction",
    "Rod Bending",
    "Surgical Workflow",
    "Modular Technology",
    "Fda 510(k) Clearance",
    "Ce Mark Approval",
    "Global Availability",
    "Clinical Evaluations",
    "Spine Procedures",
    "Surgical Efficiency",
    "Patient Outcomes"
  ],
  "regions_available": [
    "United States",
    "Europe",
    "Global"
  ],
  "languages_supported": [
    "English",
    "German",
    "French",
    "Spanish",
    "Italian",
    "Dutch",
    "Swedish",
    "Danish",
    "Norwegian",
    "Finnish",
    "Portuguese",
    "Greek",
    "Turkish",
    "Russian",
    "Polish",
    "Czech",
    "Hungarian",
    "Romanian",
    "Bulgarian",
    "Serbian",
    "Croatian"
  ],
  "pricing_model": "enterprise_quote",
  "pricing_details": "Contact vendor for pricing information.",
  "license": "commercial",
  "company_offices": [
    "United States",
    "Germany",
    "France",
    "United Kingdom",
    "Italy",
    "Spain",
    "Netherlands",
    "Sweden",
    "Denmark",
    "Norway"
  ],
  "company_founding": "1997",
  "deployment_model": [
    "on_prem"
  ],
  "os_platforms": [
    "Windows"
  ],
  "features": [
    "2D and 3D imaging and navigation",
    "Integrated Global Alignment (iGA) for surgical planning",
    "Neuromonitoring with automatic nerve detection",
    "Radiation reduction through LessRay technology",
    "Patient-specific rod bending with Bendini technology",
    "Modular architecture for flexible technology packages",
    "Wireless connectivity for seamless team collaboration",
    "Compatibility with Siemens Healthineers' Cios Spin 3D mobile C-arm"
  ],
  "optional_modules": [
    "Spine robotics module"
  ],
  "integrations": [
    "Siemens Healthineers' Cios Spin 3D mobile C-arm"
  ],
  "data_standards": [
    "HL7",
    "FHIR",
    "DICOM",
    "SNOMED",
    "ICD-10"
  ],
  "api_available": "unknown",
  "system_requirements": "Windows OS",
  "compliance": [
    "HIPAA",
    "FDA 510(k) clearance",
    "CE mark certification"
  ],
  "certifications": [
    "FDA 510(k) clearance",
    "CE mark certification"
  ],
  "security_features": [
    "Data encryption at rest and in transit",
    "Role-based access control (RBAC)",
    "Audit logs",
    "2FA"
  ],
  "privacy_features": [
    "BAA available",
    "Consent management",
    "Data anonymization",
    "Data minimization"
  ],
  "data_residency": "US-only",
  "customers": [],
  "user_reviews": [],
  "ratings": [],
  "support_channels": [],
  "training_options": [],
  "release_year": "",
  "integration_partners": [],
  "id": "SW0586",
  "slug": "pulse",
  "type": "product",
  "version": "1.0",
  "last_updated": "2025-10-11",
  "links_json": {
    "self": "https://www.healthaidb.com/software/pulse.json"
  }
}