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FDA 510(k)

EXACTECH 12/14 TOTAL HIP SYSTEM

K-Number: K041906 · 2004-09-10

Decision Date2004-09-10
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EXACTECH 12/14 TOTAL HIP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Exactech, Inc.. It received FDA 510(k) clearance on 2004-09-10 under 510(k) number K041906. 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 EXACTECH 12/14 TOTAL HIP SYSTEM?

EXACTECH 12/14 TOTAL HIP SYSTEM is a medical device that received FDA 510(k) clearance on 2004-09-10. The listed applicant is Exactech, Inc.. The 510(k) number is K041906.

When did EXACTECH 12/14 TOTAL HIP SYSTEM receive FDA 510(k) clearance?

EXACTECH 12/14 TOTAL HIP SYSTEM received FDA 510(k) clearance on 2004-09-10, under 510(k) number K041906.

Who is the listed applicant for EXACTECH 12/14 TOTAL HIP SYSTEM?

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

What is the FDA product code for EXACTECH 12/14 TOTAL HIP SYSTEM?

The FDA product code for EXACTECH 12/14 TOTAL HIP SYSTEM 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.

Other records listing Exactech, 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: 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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