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FDA 510(k)

ACUMATCH M-SERIES LPB 12/14 FEMORAL STEM

K-Number: K051858 · 2005-12-01

ApplicantExactech, Inc.
Decision Date2005-12-01
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACUMATCH M-SERIES LPB 12/14 FEMORAL STEM is the device name listed in this FDA 510(k) record. The listed applicant is Exactech, Inc.. It received FDA 510(k) clearance on 2005-12-01 under 510(k) number K051858. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACUMATCH M-SERIES LPB 12/14 FEMORAL STEM?

ACUMATCH M-SERIES LPB 12/14 FEMORAL STEM is a medical device that received FDA 510(k) clearance on 2005-12-01. The listed applicant is Exactech, Inc.. The 510(k) number is K051858.

When did ACUMATCH M-SERIES LPB 12/14 FEMORAL STEM receive FDA 510(k) clearance?

ACUMATCH M-SERIES LPB 12/14 FEMORAL STEM received FDA 510(k) clearance on 2005-12-01, under 510(k) number K051858.

Who is the listed applicant for ACUMATCH M-SERIES LPB 12/14 FEMORAL STEM?

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 ACUMATCH M-SERIES LPB 12/14 FEMORAL STEM?

The FDA product code for ACUMATCH M-SERIES LPB 12/14 FEMORAL STEM is LZO.

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Related Devices (Code: LZO)

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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