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112 devices foundsorted by relevance

Manufacturer: Nu Vasive, Incorporated Clear all

  • NuVasive® Modulus XLIF Interbody System

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Reline System

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • NuVaisve® Reline® Cervical System

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • VuePoint OCT System

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • NuVasive® VuePoint® II OCT System

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • NuVasive® Growth Rod Conversion Set

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • NuVasive Reline Fenestrated Screws, High V+ Bone Cement

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Archon Anterior Cervical Plate Syste,

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • NuVasive CoRoent Ti-C System

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • NuVasive® Interfixated Interbody System

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • NuVasive Modulus XLIF Interbody System

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • NuVasive CoRoent Thoracolumbar System

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • NuVasive NVM5 System

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • NuVasive Reline System

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Vertera Spine Cohere Cervical Interbody Fusion Device

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • NuVasive Sterilization Trays

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • NuVasive Reline Cervical System

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • NuVasive PEEK Corpectomy System

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Rod Registration Frame

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • NuVasive Next Generation NVM5 System

    Nu Vasive, Incorporated,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

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