FDA 510(k)

MSFX MIKRON PEEK 金屬網格

K 號：K252781 · 2025-12-19

申請人Mikron Makina Sanayi VE Tic. Ltd. Sti.

決定日期2025-12-19

產品代碼ODP

諮詢委員會或

決定相當於

器材摘要

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.

常見問題

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.

相關器械（代碼：ODP）

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器材摘要

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