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FDA 510(k)

M.U.S.T. MINI Posterior Cervical Screws System Extension

K-Number: K220570 · 2022-04-26

ApplicantMedacta International S.A.
Decision Date2022-04-26
Product CodeNKG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

M.U.S.T. MINI Posterior Cervical Screws System Extension is a medical device manufactured by Medacta International S.A.. It received FDA 510(k) clearance on 2022-04-26 under approval number K220570. The device is classified under product code NKG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M.U.S.T. MINI Posterior Cervical Screws System Extension?

M.U.S.T. MINI Posterior Cervical Screws System Extension is a medical device that received FDA 510(k) clearance on 2022-04-26. It is manufactured by Medacta International S.A.. The 510(k) number is K220570.

When was M.U.S.T. MINI Posterior Cervical Screws System Extension approved by the FDA?

M.U.S.T. MINI Posterior Cervical Screws System Extension received FDA 510(k) clearance on 2022-04-26, under approval number K220570.

What company makes M.U.S.T. MINI Posterior Cervical Screws System Extension?

M.U.S.T. MINI Posterior Cervical Screws System Extension is manufactured by Medacta International S.A..

What is the FDA product code for M.U.S.T. MINI Posterior Cervical Screws System Extension?

The FDA product code for M.U.S.T. MINI Posterior Cervical Screws System Extension is NKG.

Related Clinical Trials

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Related Devices (Code: NKG)

K161032neon3™ universal OCT spinal stabilizationUlrich GmbH & Co. KG K162300Reform® POCT SystemPrecision Spine, Inc. K162136CastleLoc-S Posterior Cervical Fixation System; LnK Posterior Cervical Fixation SystemL&K BIOMED Co., Ltd. K161591QUARTEX™ Occipito-Cervico-Thoracic Spinal System, Globus Navigation InstrumentsGlobus Medical, Inc. K161478Xenco Medical Posterior Cervical SystemXenco Medical, LLC K161498Streamline OCT Occipito-Cervico-Thoracic SystemPioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.)

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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