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FDA 510(k)

MSFX Mikron Cervical Anterior Plate System

K-Number: K240484 · 2024-04-17

ApplicantMikron Makina Sanayi VE Ticaret Ltd. Sti.
Decision Date2024-04-17
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MSFX Mikron Cervical Anterior Plate System is a medical device manufactured by Mikron Makina Sanayi VE Ticaret Ltd. Sti.. It received FDA 510(k) clearance on 2024-04-17 under approval number K240484. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MSFX Mikron Cervical Anterior Plate System?

MSFX Mikron Cervical Anterior Plate System is a medical device that received FDA 510(k) clearance on 2024-04-17. It is manufactured by Mikron Makina Sanayi VE Ticaret Ltd. Sti.. The 510(k) number is K240484.

When was MSFX Mikron Cervical Anterior Plate System approved by the FDA?

MSFX Mikron Cervical Anterior Plate System received FDA 510(k) clearance on 2024-04-17, under approval number K240484.

What company makes MSFX Mikron Cervical Anterior Plate System?

MSFX Mikron Cervical Anterior Plate System is manufactured by Mikron Makina Sanayi VE Ticaret Ltd. Sti..

What is the FDA product code for MSFX Mikron Cervical Anterior Plate System?

The FDA product code for MSFX Mikron Cervical Anterior Plate System is KWQ.

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Other Devices by Mikron Makina Sanayi VE Ticaret Ltd. Sti.

K241657MSFX MIKRON SPINAL FIXATION SYSTEM

Related Devices (Code: KWQ)

K160982Sphynx™Eden Spine, LLC K162638CETRA Anterior Cervical Plate SystemOrthofix, Inc. K162194MEDICREA INTERNATIONAL Anterior Cervical Locking Plate SystemMedicrea International SA K162211AccuFit Lateral Plate SystemPrecision Spine, Inc. K162250FortiBridge Anterior Cervical Plate SystemNanovis Spine, LLC K162664Pyrenees Cervical Plate SystemK2m, 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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