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FDA 510(k)

HPS II CALCAR FEMORAL PROSTHESIS

K-Number: K871857 · 1987-06-23

ApplicantDepuy, Inc.
Decision Date1987-06-23
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

HPS II CALCAR FEMORAL PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1987-06-23 under 510(k) number K871857. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the HPS II CALCAR FEMORAL PROSTHESIS?

HPS II CALCAR FEMORAL PROSTHESIS is a medical device that received FDA 510(k) clearance on 1987-06-23. The listed applicant is Depuy, Inc.. The 510(k) number is K871857.

When did HPS II CALCAR FEMORAL PROSTHESIS receive FDA 510(k) clearance?

HPS II CALCAR FEMORAL PROSTHESIS received FDA 510(k) clearance on 1987-06-23, under 510(k) number K871857.

Who is the listed applicant for HPS II CALCAR FEMORAL PROSTHESIS?

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 HPS II CALCAR FEMORAL PROSTHESIS?

The FDA product code for HPS II CALCAR FEMORAL PROSTHESIS is JDI.

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Other records listing Depuy, Inc. as applicant

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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Related Devices (Code: JDI)

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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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