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FDA 510(k)

ANATOMICAL SHOULDER INVERSE/REVERSE

K-Number: K053274 · 2006-01-25

ApplicantZimmer GmbH
Decision Date2006-01-25
Product CodePHX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ANATOMICAL SHOULDER INVERSE/REVERSE is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer GmbH. It received FDA 510(k) clearance on 2006-01-25 under 510(k) number K053274. The device is classified under product code PHX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANATOMICAL SHOULDER INVERSE/REVERSE?

ANATOMICAL SHOULDER INVERSE/REVERSE is a medical device that received FDA 510(k) clearance on 2006-01-25. The listed applicant is Zimmer GmbH. The 510(k) number is K053274.

When did ANATOMICAL SHOULDER INVERSE/REVERSE receive FDA 510(k) clearance?

ANATOMICAL SHOULDER INVERSE/REVERSE received FDA 510(k) clearance on 2006-01-25, under 510(k) number K053274.

Who is the listed applicant for ANATOMICAL SHOULDER INVERSE/REVERSE?

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

What is the FDA product code for ANATOMICAL SHOULDER INVERSE/REVERSE?

The FDA product code for ANATOMICAL SHOULDER INVERSE/REVERSE is PHX.

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Related Devices (Code: PHX)

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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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