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FDA 510(k)

GLOBAL CAP RESURFACING REPLACEMENT SHOULDER

K-Number: K031971 · 2003-09-24

ApplicantDePuy Orthopaedics, Inc.
Decision Date2003-09-24
Product CodeHSD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

GLOBAL CAP RESURFACING REPLACEMENT 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 2003-09-24 under 510(k) number K031971. 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 GLOBAL CAP RESURFACING REPLACEMENT SHOULDER?

GLOBAL CAP RESURFACING REPLACEMENT SHOULDER is a medical device that received FDA 510(k) clearance on 2003-09-24. The listed applicant is DePuy Orthopaedics, Inc.. The 510(k) number is K031971.

When did GLOBAL CAP RESURFACING REPLACEMENT SHOULDER receive FDA 510(k) clearance?

GLOBAL CAP RESURFACING REPLACEMENT SHOULDER received FDA 510(k) clearance on 2003-09-24, under 510(k) number K031971.

Who is the listed applicant for GLOBAL CAP RESURFACING REPLACEMENT 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 GLOBAL CAP RESURFACING REPLACEMENT SHOULDER?

The FDA product code for GLOBAL CAP RESURFACING REPLACEMENT SHOULDER is HSD.

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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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