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FDA 510(k)

ANTERIOR KYPHOSIS DISTRACTION DEVICE

K-Number: K802222 · 1980-10-10

ApplicantZimmer, Inc.
Decision Date1980-10-10
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ANTERIOR KYPHOSIS DISTRACTION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1980-10-10 under 510(k) number K802222. 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 ANTERIOR KYPHOSIS DISTRACTION DEVICE?

ANTERIOR KYPHOSIS DISTRACTION DEVICE is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is Zimmer, Inc.. The 510(k) number is K802222.

When did ANTERIOR KYPHOSIS DISTRACTION DEVICE receive FDA 510(k) clearance?

ANTERIOR KYPHOSIS DISTRACTION DEVICE received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802222.

Who is the listed applicant for ANTERIOR KYPHOSIS DISTRACTION DEVICE?

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

What is the FDA product code for ANTERIOR KYPHOSIS DISTRACTION DEVICE?

The FDA product code for ANTERIOR KYPHOSIS DISTRACTION DEVICE 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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