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FDA 510(k)

INVIZIA ANTERIOR CERVICAL PLATE SYSTEM

K-Number: K111796 · 2011-10-27

ApplicantZimmer Spine, Inc.
Decision Date2011-10-27
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INVIZIA ANTERIOR CERVICAL PLATE 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 2011-10-27 under 510(k) number K111796. 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 INVIZIA ANTERIOR CERVICAL PLATE SYSTEM?

INVIZIA ANTERIOR CERVICAL PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2011-10-27. The listed applicant is Zimmer Spine, Inc.. The 510(k) number is K111796.

When did INVIZIA ANTERIOR CERVICAL PLATE SYSTEM receive FDA 510(k) clearance?

INVIZIA ANTERIOR CERVICAL PLATE SYSTEM received FDA 510(k) clearance on 2011-10-27, under 510(k) number K111796.

Who is the listed applicant for INVIZIA ANTERIOR CERVICAL PLATE 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 INVIZIA ANTERIOR CERVICAL PLATE SYSTEM?

The FDA product code for INVIZIA ANTERIOR CERVICAL PLATE 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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