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VuePoint OCT Plate, Keel - SFDA Registration ME0000005437SFDAA00220

Access comprehensive regulatory information for VuePoint OCT Plate, Keel in the Saudi Arabia medical device market through Pure Global AI's free database. This Class II device is registered with Saudi Arabia SFDA under registration number ME0000005437SFDAA00220 and manufactured by NuVasive Inc..

This page provides complete registration details including product category (MD), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.

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Class II
ME0000005437SFDAA00220
VuePoint OCT Plate, Keel
SFDA Registration: ME0000005437SFDAA00220
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Product Information

The NuVasive VuePoint II OCT System consists of screws, hooks, rods, offset connectors, rod to rod connectors, set screws, cross connectors, occipital plates and associated general instruments. Implant components are available in a variety sizes and can be rigidly locked into a variety of configurations to suit the individual pathology and anatomical conditions of the patient. The scope of this submission includes the introduction of 5.0 and 5.5 mm diameter multi axial bone screws, sterile implants, as well as minor modifications to the implant design since clearance of reference device NuVasive VuePoint II OCT System (K150474).

Product Use

The NuVasive VuePoint OCT System and NuVasive VuePoint II OCT System are intended to provide immobilization and stabilization of spinal segments as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical junction, the cervical spine (C1 to C7) and the thoracic spine (T1-T3): traumatic spinal fractures and/or traumatic dislocations; instability or deformity; failed previous fusions (e.g., pseudoarthrosis); tumors involving the cervical spine; and degenerative disease, including intractable radiculopathy and/or myelopathy, neck and/or arm pain of discogenic origin as confirmed by radiographic studies, and degenerative disease of the facets with instability.

Device Classification
Risk Class
Class II
Product Category
MD
Product Type
MD
Registration Information
Registration ID
ME0000005437SFDAA00220
Authorization ID
MDMA-1-2019-5839
Status
Active
Expire Date
November 19, 2025
Manufacturer
Manufacturer Name
NuVasive Inc.
Model Information
Model ID(s)
7906335 7906340 7906345
Product Accessories

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