Hammerdesis™ 間指融合系統
K 號：K231147 · 2023-09-14
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器材摘要
Hammerdesis™ Interphalangeal Fusion System is the device name listed in this FDA 510(k) record. The listed applicant is Intelivation. It received FDA 510(k) clearance on 2023-09-14 under 510(k) number K231147. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Hammerdesis™ Interphalangeal Fusion System?
Hammerdesis™ Interphalangeal Fusion System is a medical device that received FDA 510(k) clearance on 2023-09-14. The listed applicant is Intelivation. The 510(k) number is K231147.
When did Hammerdesis™ Interphalangeal Fusion System receive FDA 510(k) clearance?
Hammerdesis™ Interphalangeal Fusion System received FDA 510(k) clearance on 2023-09-14, under 510(k) number K231147.
Who is the listed applicant for Hammerdesis™ Interphalangeal Fusion System?
The FDA 510(k) record lists Intelivation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Hammerdesis™ Interphalangeal Fusion System?
The FDA product code for Hammerdesis™ Interphalangeal Fusion System is HTY.
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相關器械（代碼：HTY）
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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