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FDA 510(k)

DEPUY GLOBAL C.AP. CTA RESURFACING SHOULDER

K-Number: K080990 · 2008-08-08

ApplicantDePuy Orthopaedics, Inc.
Decision Date2008-08-08
Product CodeHSD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DEPUY GLOBAL C.AP. CTA RESURFACING SHOULDER is the device name listed in this FDA 510(k) record. The listed applicant is DePuy Orthopaedics, Inc.. It received FDA 510(k) clearance on 2008-08-08 under 510(k) number K080990. The device is classified under product code HSD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEPUY GLOBAL C.AP. CTA RESURFACING SHOULDER?

DEPUY GLOBAL C.AP. CTA RESURFACING SHOULDER is a medical device that received FDA 510(k) clearance on 2008-08-08. The listed applicant is DePuy Orthopaedics, Inc.. The 510(k) number is K080990.

When did DEPUY GLOBAL C.AP. CTA RESURFACING SHOULDER receive FDA 510(k) clearance?

DEPUY GLOBAL C.AP. CTA RESURFACING SHOULDER received FDA 510(k) clearance on 2008-08-08, under 510(k) number K080990.

Who is the listed applicant for DEPUY GLOBAL C.AP. CTA RESURFACING SHOULDER?

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

What is the FDA product code for DEPUY GLOBAL C.AP. CTA RESURFACING SHOULDER?

The FDA product code for DEPUY GLOBAL C.AP. CTA RESURFACING SHOULDER is HSD.

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Other records listing DePuy Orthopaedics, Inc. as applicant

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Related Devices (Code: HSD)

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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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