Polymeric spinal interbody fusion cage - UK MHRA Medical Device Registration

Polymeric spinal interbody fusion cage is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 86520. The device is manufactured by NuVasive Inc. from United States, classified as General Medical Device. The authorized representative in the UK is NuVasive UK Limited.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Polymeric spinal interbody fusion cage

MHRA Device ID: 86520•Ref: 86520

Device Type

General Medical Device

Devices

Polymeric spinal interbody fusion cage

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Feb 23, 2024

Manufacturer Information

Name

NuVasive Inc.

Address

7475 Lusk Blvd, San Diego, CA 92121, United States

San Diego, United States

Created Date

Feb 23, 2021

Authorized Representative

Name

NuVasive UK Limited

Relationship Type

UK Responsible Person

Address

Suite B, Ground Floor, Caspian House, The Waterfront, Elstree

London, Hertfordshire, England, United Kingdom

Postcode: WD63BS

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Polymeric spinal interbody fusion cage - UK MHRA Medical Device Registration

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Date Registered

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