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FDA 510(k)

Persona 個人化膝關節系統(Persona 多孔等离子喷涂 PPS 髋骨)

K 號:K253189 · 2026-03-09

申請人Zimmer, Inc.
決定日期2026-03-09
產品代碼MBH
諮詢委員會或
決定相當於

器材摘要

Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs) is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2026-03-09 under 510(k) number K253189. The device is classified under product code MBH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs)?

Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs) is a medical device that received FDA 510(k) clearance on 2026-03-09. The listed applicant is Zimmer, Inc.. The 510(k) number is K253189.

When did Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs) receive FDA 510(k) clearance?

Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs) received FDA 510(k) clearance on 2026-03-09, under 510(k) number K253189.

Who is the listed applicant for Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs)?

FDA 510(k) 記錄將 Zimmer, Inc. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs)?

The FDA product code for Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs) is MBH.

相關臨床試驗

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其他以 Zimmer, Inc. 為申請人之記錄

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相關器械(代碼:MBH)

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。

官方來源

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