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FDA 510(k)

NUVASIVE TOWNLEY FACET SCREW

K-Number: K994308 · 2000-04-18

ApplicantNuvasive, Inc.
Decision Date2000-04-18
Product CodeMRW
DecisionSubstantially Equivalent

Device Summary

NUVASIVE TOWNLEY FACET SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Nuvasive, Inc.. It received FDA 510(k) clearance on 2000-04-18 under 510(k) number K994308. The device is classified under product code MRW. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUVASIVE TOWNLEY FACET SCREW?

NUVASIVE TOWNLEY FACET SCREW is a medical device that received FDA 510(k) clearance on 2000-04-18. The listed applicant is Nuvasive, Inc.. The 510(k) number is K994308.

When did NUVASIVE TOWNLEY FACET SCREW receive FDA 510(k) clearance?

NUVASIVE TOWNLEY FACET SCREW received FDA 510(k) clearance on 2000-04-18, under 510(k) number K994308.

Who is the listed applicant for NUVASIVE TOWNLEY FACET SCREW?

The FDA 510(k) record lists Nuvasive, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NUVASIVE TOWNLEY FACET SCREW?

The FDA product code for NUVASIVE TOWNLEY FACET SCREW is MRW.

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Related Devices (Code: MRW)

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K262618Arthrex Spine Compression FT ScrewArthrex, Inc.K261209Ion-LSurGenTec, LLCK253676CORUS™ Posterior Cervical Stabilization System 3D (CORUS™ PCSS 3D)Providence Medical Technology, Inc.K253432DiversiVy™ Facet Screw SystemVy Spine, LLCK251714Ion-CSurGenTec, LLCK250679FFX Facet Fixation SystemSc Medica

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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