MSFX MIKRON PEEK CAGES
K-Number: K252781 · 2025-12-19
Decision Date2025-12-19
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
MSFX MIKRON PEEK CAGES is a medical device manufactured by Mikron Makina Sanayi VE Tic. Ltd. Sti.. It received FDA 510(k) clearance on 2025-12-19 under approval 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. It is manufactured by Mikron Makina Sanayi VE Tic. Ltd. Sti.. The 510(k) number is K252781.
When was MSFX MIKRON PEEK CAGES approved by the FDA?
MSFX MIKRON PEEK CAGES received FDA 510(k) clearance on 2025-12-19, under approval number K252781.
What company makes MSFX MIKRON PEEK CAGES?
MSFX MIKRON PEEK CAGES is manufactured by Mikron Makina Sanayi VE Tic. Ltd. Sti..
What is the FDA product code for MSFX MIKRON PEEK CAGES?
The FDA product code for MSFX MIKRON PEEK CAGES is ODP.
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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.