FDA 510(k)

Libertas 縮窄短 (TS) 未固定股骨柄 (Libertas TS 柄)

K 號：K253171 · 2026-01-15

決定日期2026-01-15

產品代碼LZO

諮詢委員會或

決定相當於

器材摘要

Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem) is the device name listed in this FDA 510(k) record. The listed applicant is Maxx Orthopedics, Inc.. It received FDA 510(k) clearance on 2026-01-15 under 510(k) number K253171. 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 Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)?

Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem) is a medical device that received FDA 510(k) clearance on 2026-01-15. The listed applicant is Maxx Orthopedics, Inc.. The 510(k) number is K253171.

When did Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem) receive FDA 510(k) clearance?

Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem) received FDA 510(k) clearance on 2026-01-15, under 510(k) number K253171.

Who is the listed applicant for Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)?

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

What is the FDA product code for Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)?

The FDA product code for Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem) is LZO.

其他以 Maxx Orthopedics, Inc. 為申請人之記錄

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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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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