明尼蒂斯MMF縫合系統
K 號：K162046 · 2017-04-11
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器材摘要
MINNE TIES MMF Suture System is the device name listed in this FDA 510(k) record. The listed applicant is Summit Medical, Inc.. It received FDA 510(k) clearance on 2017-04-11 under 510(k) number K162046. The device is classified under product code DYX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MINNE TIES MMF Suture System?
MINNE TIES MMF Suture System is a medical device that received FDA 510(k) clearance on 2017-04-11. The listed applicant is Summit Medical, Inc.. The 510(k) number is K162046.
When did MINNE TIES MMF Suture System receive FDA 510(k) clearance?
MINNE TIES MMF Suture System received FDA 510(k) clearance on 2017-04-11, under 510(k) number K162046.
Who is the listed applicant for MINNE TIES MMF Suture System?
The FDA 510(k) record lists Summit Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MINNE TIES MMF Suture System?
The FDA product code for MINNE TIES MMF Suture System is DYX.
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其他以 Summit Medical, 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。
官方來源
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