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FDA 510(k)

MODIFICATION TO ESOP CO-CR FEMORAL HEADS

K-Number: K023375 · 2002-10-25

Decision Date2002-10-25
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO ESOP CO-CR FEMORAL HEADS is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Active Healthcare. It received FDA 510(k) clearance on 2002-10-25 under 510(k) number K023375. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO ESOP CO-CR FEMORAL HEADS?

MODIFICATION TO ESOP CO-CR FEMORAL HEADS is a medical device that received FDA 510(k) clearance on 2002-10-25. The listed applicant is Pro-Active Healthcare. The 510(k) number is K023375.

When did MODIFICATION TO ESOP CO-CR FEMORAL HEADS receive FDA 510(k) clearance?

MODIFICATION TO ESOP CO-CR FEMORAL HEADS received FDA 510(k) clearance on 2002-10-25, under 510(k) number K023375.

Who is the listed applicant for MODIFICATION TO ESOP CO-CR FEMORAL HEADS?

The FDA 510(k) record lists Pro-Active Healthcare as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION TO ESOP CO-CR FEMORAL HEADS?

The FDA product code for MODIFICATION TO ESOP CO-CR FEMORAL HEADS is LPH.

Related Clinical Trials

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.

Related Devices (Code: LPH)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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