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FDA 510(k)

V2F ANTERIOR FIXATION SYSTEM

K-Number: K122733 · 2012-12-07

ApplicantZimmer Spine, Inc.
Decision Date2012-12-07
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

V2F ANTERIOR FIXATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Spine, Inc.. It received FDA 510(k) clearance on 2012-12-07 under 510(k) number K122733. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V2F ANTERIOR FIXATION SYSTEM?

V2F ANTERIOR FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 2012-12-07. The listed applicant is Zimmer Spine, Inc.. The 510(k) number is K122733.

When did V2F ANTERIOR FIXATION SYSTEM receive FDA 510(k) clearance?

V2F ANTERIOR FIXATION SYSTEM received FDA 510(k) clearance on 2012-12-07, under 510(k) number K122733.

Who is the listed applicant for V2F ANTERIOR FIXATION SYSTEM?

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

What is the FDA product code for V2F ANTERIOR FIXATION SYSTEM?

The FDA product code for V2F ANTERIOR FIXATION SYSTEM is KWQ.

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Related Devices (Code: KWQ)

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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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