MODIFICATION TO ESOP CO-CR FEMORAL HEADS
K-Number: K023375 · 2002-10-25
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Device Summary
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
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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