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FDA 510(k)

M.U.S.T. Combined Set Screws

K-Number: K171758 · 2017-08-01

ApplicantMedacta International S.A.
Decision Date2017-08-01
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

M.U.S.T. Combined Set Screws is the device name listed in this FDA 510(k) record. The listed applicant is Medacta International S.A.. It received FDA 510(k) clearance on 2017-08-01 under 510(k) number K171758. 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. Combined Set Screws?

M.U.S.T. Combined Set Screws is a medical device that received FDA 510(k) clearance on 2017-08-01. The listed applicant is Medacta International S.A.. The 510(k) number is K171758.

When did M.U.S.T. Combined Set Screws receive FDA 510(k) clearance?

M.U.S.T. Combined Set Screws received FDA 510(k) clearance on 2017-08-01, under 510(k) number K171758.

Who is the listed applicant for M.U.S.T. Combined Set Screws?

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

What is the FDA product code for M.U.S.T. Combined Set Screws?

The FDA product code for M.U.S.T. Combined Set Screws is NKB.

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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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