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FDA 510(k)

MSFX MIKRON PEEK CAGES

K-Number: K252781 · 2025-12-19

ApplicantMikron Makina Sanayi VE Tic. Ltd. Sti.
Decision Date2025-12-19
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MSFX MIKRON PEEK CAGES is the device name listed in this FDA 510(k) record. The listed applicant is Mikron Makina Sanayi VE Tic. Ltd. Sti.. It received FDA 510(k) clearance on 2025-12-19 under 510(k) number K252781. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MSFX MIKRON PEEK CAGES?

MSFX MIKRON PEEK CAGES is a medical device that received FDA 510(k) clearance on 2025-12-19. The listed applicant is Mikron Makina Sanayi VE Tic. Ltd. Sti.. The 510(k) number is K252781.

When did MSFX MIKRON PEEK CAGES receive FDA 510(k) clearance?

MSFX MIKRON PEEK CAGES received FDA 510(k) clearance on 2025-12-19, under 510(k) number K252781.

Who is the listed applicant for MSFX MIKRON PEEK CAGES?

The FDA 510(k) record lists Mikron Makina Sanayi VE Tic. Ltd. Sti. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MSFX MIKRON PEEK CAGES?

The FDA product code for MSFX MIKRON PEEK CAGES is ODP.

Related Devices (Code: ODP)

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.

K2530413d Cage CervicalFims Co., Ltd.K262061Tritanium® C Anterior Cervical Cage; Tritanium® PL Cage; Tritanium® TL Curved Posterior Lumbar Cage; Aero® -C Cervical Cage System; AVS® Anchor-C Cervical Cage System; AVS® TL PEEK Spacer; AVS® PL PEEK Spacers; AVS® Navigator PEEK Spacer; AVS® AS PEEK Spacer; Monterey™ AL Interbody System; Aleutian IBF System; Cascadia Interbody System; Chesapeake Stabilization System; Sahara Stabilization System; SANTORINI™ Corpectomy Cage System; MOJAVE Interbody System; VLIFT VERTEBRAL BODY REPLACEMStryker SpineK254130C.A. Medical Interbody Fusion SystemC.A. Medical, LLCK260840BluEX Cervical Expandable Cage SystemL&K BIOMED Co., Ltd.K260850OSTEOMNI SPINAL CAGES SYSTEMOsteomni, Inc.K260549ZSFab Cervical Interbody System and ZSFab Lumbar Interbody SystemZsfab, 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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