EXACTECH ACUMATCH A-SERIES & MCS CONSTRAINED ACETABULAR LINERS
K-Number: K040601 · 2004-10-04
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Device Summary
Frequently Asked Questions
What is the EXACTECH ACUMATCH A-SERIES & MCS CONSTRAINED ACETABULAR LINERS?
EXACTECH ACUMATCH A-SERIES & MCS CONSTRAINED ACETABULAR LINERS is a medical device that received FDA 510(k) clearance on 2004-10-04. The listed applicant is Exactech, Inc.. The 510(k) number is K040601.
When did EXACTECH ACUMATCH A-SERIES & MCS CONSTRAINED ACETABULAR LINERS receive FDA 510(k) clearance?
EXACTECH ACUMATCH A-SERIES & MCS CONSTRAINED ACETABULAR LINERS received FDA 510(k) clearance on 2004-10-04, under 510(k) number K040601.
Who is the listed applicant for EXACTECH ACUMATCH A-SERIES & MCS CONSTRAINED ACETABULAR LINERS?
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 ACUMATCH A-SERIES & MCS CONSTRAINED ACETABULAR LINERS?
The FDA product code for EXACTECH ACUMATCH A-SERIES & MCS CONSTRAINED ACETABULAR LINERS is KWZ.
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.
Related Devices (Code: KWZ)
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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