FDA 510(k)

Corin最佳定位系統 (OPS) 髋部

K 號：K193545 · 2020-08-04

決定日期2020-08-04

產品代碼LZO

諮詢委員會或

決定相當於

器材摘要

Corin Optimized Positioning System (OPS) Femoral is the device name listed in this FDA 510(k) record. The listed applicant is Corin USA. It received FDA 510(k) clearance on 2020-08-04 under 510(k) number K193545. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Corin Optimized Positioning System (OPS) Femoral?

Corin Optimized Positioning System (OPS) Femoral is a medical device that received FDA 510(k) clearance on 2020-08-04. The listed applicant is Corin USA. The 510(k) number is K193545.

When did Corin Optimized Positioning System (OPS) Femoral receive FDA 510(k) clearance?

Corin Optimized Positioning System (OPS) Femoral received FDA 510(k) clearance on 2020-08-04, under 510(k) number K193545.

Who is the listed applicant for Corin Optimized Positioning System (OPS) Femoral?

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

What is the FDA product code for Corin Optimized Positioning System (OPS) Femoral?

The FDA product code for Corin Optimized Positioning System (OPS) Femoral is LZO.

其他以 Corin USA 為申請人之記錄

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相關器械（代碼：LZO）

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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