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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 a medical device manufactured by Medacta International S.A.. It received FDA 510(k) clearance on 2017-08-01 under approval 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. It is manufactured by Medacta International S.A.. The 510(k) number is K171758.

When was M.U.S.T. Combined Set Screws approved by the FDA?

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

What company makes M.U.S.T. Combined Set Screws?

M.U.S.T. Combined Set Screws is manufactured by Medacta International S.A..

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.

Related Clinical Trials

NCT07408726 Monoaxial vs. Polyaxial Percutaneous Hybrid Stabilization NOT_YET_RECRUITING

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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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