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FDA 510(k)

CONTOUR FEMORAL HIP STEM W/HYDROAPATITE COATING

K-Number: K926299 · 1993-10-22

ApplicantDepuy, Inc.
Decision Date1993-10-22
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONTOUR FEMORAL HIP STEM W/HYDROAPATITE COATING is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1993-10-22 under 510(k) number K926299. The device is classified under product code MEH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTOUR FEMORAL HIP STEM W/HYDROAPATITE COATING?

CONTOUR FEMORAL HIP STEM W/HYDROAPATITE COATING is a medical device that received FDA 510(k) clearance on 1993-10-22. The listed applicant is Depuy, Inc.. The 510(k) number is K926299.

When did CONTOUR FEMORAL HIP STEM W/HYDROAPATITE COATING receive FDA 510(k) clearance?

CONTOUR FEMORAL HIP STEM W/HYDROAPATITE COATING received FDA 510(k) clearance on 1993-10-22, under 510(k) number K926299.

Who is the listed applicant for CONTOUR FEMORAL HIP STEM W/HYDROAPATITE COATING?

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

What is the FDA product code for CONTOUR FEMORAL HIP STEM W/HYDROAPATITE COATING?

The FDA product code for CONTOUR FEMORAL HIP STEM W/HYDROAPATITE COATING is MEH.

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Other records listing Depuy, Inc. as applicant

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Related Devices (Code: MEH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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