FDA 510(k)

SIGNAFUSE 生物活性條 (SBS)；SIGNAFUSE 黏土

K 號：K233490 · 2023-12-05

決定日期2023-12-05

產品代碼MQV

諮詢委員會或

決定相當於

器材摘要

SIGNAFUSE Bioactive Strip (SBS); SIGNAFUSE Putty is the device name listed in this FDA 510(k) record. The listed applicant is Bioventus, LLC. It received FDA 510(k) clearance on 2023-12-05 under 510(k) number K233490. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the SIGNAFUSE Bioactive Strip (SBS); SIGNAFUSE Putty?

SIGNAFUSE Bioactive Strip (SBS); SIGNAFUSE Putty is a medical device that received FDA 510(k) clearance on 2023-12-05. The listed applicant is Bioventus, LLC. The 510(k) number is K233490.

When did SIGNAFUSE Bioactive Strip (SBS); SIGNAFUSE Putty receive FDA 510(k) clearance?

SIGNAFUSE Bioactive Strip (SBS); SIGNAFUSE Putty received FDA 510(k) clearance on 2023-12-05, under 510(k) number K233490.

Who is the listed applicant for SIGNAFUSE Bioactive Strip (SBS); SIGNAFUSE Putty?

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

What is the FDA product code for SIGNAFUSE Bioactive Strip (SBS); SIGNAFUSE Putty?

The FDA product code for SIGNAFUSE Bioactive Strip (SBS); SIGNAFUSE Putty is MQV.

其他以 Bioventus, LLC 為申請人之記錄

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相關器械（代碼：MQV）

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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