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FDA 510(k)

Precice™ Max 系統及 Precice™ 腳踝挽救系統

K 號:K261651 · 2026-06-18

決定日期2026-06-18
產品代碼HSB
諮詢委員會或
決定相當於

器材摘要

Precice™ Max System and Precice™ Ankle Salvage System is the device name listed in this FDA 510(k) record. The listed applicant is NuVasive Specialized Orthopedics. It received FDA 510(k) clearance on 2026-06-18 under 510(k) number K261651. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Precice™ Max System and Precice™ Ankle Salvage System?

Precice™ Max System and Precice™ Ankle Salvage System is a medical device that received FDA 510(k) clearance on 2026-06-18. The listed applicant is NuVasive Specialized Orthopedics. The 510(k) number is K261651.

When did Precice™ Max System and Precice™ Ankle Salvage System receive FDA 510(k) clearance?

Precice™ Max System and Precice™ Ankle Salvage System received FDA 510(k) clearance on 2026-06-18, under 510(k) number K261651.

Who is the listed applicant for Precice™ Max System and Precice™ Ankle Salvage System?

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

What is the FDA product code for Precice™ Max System and Precice™ Ankle Salvage System?

The FDA product code for Precice™ Max System and Precice™ Ankle Salvage System is HSB.

相關臨床試驗

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相關器械(代碼:HSB)

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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