人工義肢，手指，限制性，金屬/聚合物
PMA 核准號：P960053 · 2016-08-09
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器材摘要
Prosthesis, finger, constrained, metal/polymer is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corporation. It received FDA 510(k) clearance on 2016-08-09. The device is classified under product code KWG. It was reviewed by the OR advisory panel.
常見問題
What is the Prosthesis, finger, constrained, metal/polymer?
Prosthesis, finger, constrained, metal/polymer is a medical device that received FDA 510(k) clearance on 2016-08-09. The listed applicant is Stryker Corporation.
When did Prosthesis, finger, constrained, metal/polymer receive FDA 510(k) clearance?
The clearance date for Prosthesis, finger, constrained, metal/polymer can be found in the official FDA records.
Who is the listed applicant for Prosthesis, finger, constrained, metal/polymer?
The FDA 510(k) record lists Stryker Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Prosthesis, finger, constrained, metal/polymer?
The FDA product code for Prosthesis, finger, constrained, metal/polymer is KWG.
相關臨床試驗
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官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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