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FDA 510(k)

ProGrip™ 自粘性聚丙烯網

K 號:K243315 · 2025-01-17

決定日期2025-01-17
產品代碼FTL
諮詢委員會SU 請提供完整的描述文本,以便我進行翻譯。
決定相當於

器材摘要

ProGrip™ Self-Gripping Polypropylene Mesh is the device name listed in this FDA 510(k) record. The listed applicant is Sofradim Production. It received FDA 510(k) clearance on 2025-01-17 under 510(k) number K243315. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ProGrip™ Self-Gripping Polypropylene Mesh?

ProGrip™ Self-Gripping Polypropylene Mesh is a medical device that received FDA 510(k) clearance on 2025-01-17. The listed applicant is Sofradim Production. The 510(k) number is K243315.

When did ProGrip™ Self-Gripping Polypropylene Mesh receive FDA 510(k) clearance?

ProGrip™ Self-Gripping Polypropylene Mesh received FDA 510(k) clearance on 2025-01-17, under 510(k) number K243315.

Who is the listed applicant for ProGrip™ Self-Gripping Polypropylene Mesh?

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

What is the FDA product code for ProGrip™ Self-Gripping Polypropylene Mesh?

The FDA product code for ProGrip™ Self-Gripping Polypropylene Mesh is FTL.

相關臨床試驗

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其他以 Sofradim Production 為申請人之記錄

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相關器械(代碼:FTL)

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係,請查閱連結的官方來源。

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