Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing
PMA 核准號：P830055 · 2026-09-25
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器材摘要
Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 2026-09-25. The device is classified under product code NJL. It was reviewed by the OR advisory panel.
常見問題
What is the Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing?
Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing is a medical device that received FDA 510(k) clearance on 2026-09-25. The listed applicant is Depuy, Inc..
When did Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing receive FDA 510(k) clearance?
The clearance date for Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing can be found in the official FDA records.
Who is the listed applicant for Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing?
The FDA 510(k) record lists Depuy, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing?
The FDA product code for Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing is NJL.
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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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