FDA 510(k)

MOD-C (請注意：此為簡化翻譯，具體內容可能需要根據實際情境進行調整。)

K 號：K242303 · 2026-04-01

決定日期2026-04-01

產品代碼ODP

諮詢委員會或

決定相當於

器材摘要

MOD-C is the device name listed in this FDA 510(k) record. The listed applicant is Orthomod, LLC. It received FDA 510(k) clearance on 2026-04-01 under 510(k) number K242303. 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 MOD-C?

MOD-C is a medical device that received FDA 510(k) clearance on 2026-04-01. The listed applicant is Orthomod, LLC. The 510(k) number is K242303.

When did MOD-C receive FDA 510(k) clearance?

MOD-C received FDA 510(k) clearance on 2026-04-01, under 510(k) number K242303.

Who is the listed applicant for MOD-C?

The FDA 510(k) record lists Orthomod, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOD-C?

The FDA product code for MOD-C is ODP.

相關器械（代碼：ODP）

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官方來源

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