FDA 510(k)

NovaBone Putty - 合成生物活性骨移植材

K 號：K242299 · 2024-09-25

決定日期2024-09-25

產品代碼MQV

諮詢委員會或

決定相當於

器材摘要

NovaBone Putty - Synthetic Bioactive Bone Graft is the device name listed in this FDA 510(k) record. The listed applicant is Novabone Products, LLC. It received FDA 510(k) clearance on 2024-09-25 under 510(k) number K242299. 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 NovaBone Putty - Synthetic Bioactive Bone Graft?

NovaBone Putty - Synthetic Bioactive Bone Graft is a medical device that received FDA 510(k) clearance on 2024-09-25. The listed applicant is Novabone Products, LLC. The 510(k) number is K242299.

When did NovaBone Putty - Synthetic Bioactive Bone Graft receive FDA 510(k) clearance?

NovaBone Putty - Synthetic Bioactive Bone Graft received FDA 510(k) clearance on 2024-09-25, under 510(k) number K242299.

Who is the listed applicant for NovaBone Putty - Synthetic Bioactive Bone Graft?

The FDA 510(k) record lists Novabone Products, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NovaBone Putty - Synthetic Bioactive Bone Graft?

The FDA product code for NovaBone Putty - Synthetic Bioactive Bone Graft is MQV.

其他以 Novabone Products, LLC 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。

K240404NovaBone Putty - 生物活性合成骨移植材 (NB6600, NB6610, NB6615)K220498NovoGen 瘘口網絡 K163310諾瓦骨IRM

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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