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FDA 510(k)

M.U.S.T. EXTENSION

K-Number: K132878 · 2013-12-18

ApplicantMedacta International
Decision Date2013-12-18
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

M.U.S.T. EXTENSION is the device name listed in this FDA 510(k) record. The listed applicant is Medacta International. It received FDA 510(k) clearance on 2013-12-18 under 510(k) number K132878. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M.U.S.T. EXTENSION?

M.U.S.T. EXTENSION is a medical device that received FDA 510(k) clearance on 2013-12-18. The listed applicant is Medacta International. The 510(k) number is K132878.

When did M.U.S.T. EXTENSION receive FDA 510(k) clearance?

M.U.S.T. EXTENSION received FDA 510(k) clearance on 2013-12-18, under 510(k) number K132878.

Who is the listed applicant for M.U.S.T. EXTENSION?

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

What is the FDA product code for M.U.S.T. EXTENSION?

The FDA product code for M.U.S.T. EXTENSION is NKB.

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Other records listing Medacta International as applicant

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Related Devices (Code: NKB)

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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