FDA 510(k)

Vista BC Putty

K 號：K241457 · 2024-08-28

決定日期2024-08-28

產品代碼KIF

諮詢委員會DE

決定相當於

器材摘要

Vista BC Putty is the device name listed in this FDA 510(k) record. The listed applicant is Inter-Med, Inc.. It received FDA 510(k) clearance on 2024-08-28 under 510(k) number K241457. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Vista BC Putty?

Vista BC Putty is a medical device that received FDA 510(k) clearance on 2024-08-28. The listed applicant is Inter-Med, Inc.. The 510(k) number is K241457.

When did Vista BC Putty receive FDA 510(k) clearance?

Vista BC Putty received FDA 510(k) clearance on 2024-08-28, under 510(k) number K241457.

Who is the listed applicant for Vista BC Putty?

The FDA 510(k) record lists Inter-Med, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vista BC Putty?

The FDA product code for Vista BC Putty is KIF.

其他以 Inter-Med, 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。

K253337REGEN 生物活性水泥 K241489ReminGel K241354密封劑溶劑 K221811Vista BC 密封機 K211721PS系統

相關器械（代碼：KIF）

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。

K262050Vioseal XSpident Co., Ltd.K253909NeoPEX™ 預混充填膠NuSmile, Ltd.K261514鈣氫氧化臨時填充材質（KP-Cal）Guilin Kevin Peter Technology Co., Ltd.K261415注射式根管封閉劑（KP-Root SP）Guilin Kevin Peter Technology Co., Ltd.K253167Any-PasteMediclus Co., Ltd.K252890ZenSeal ProKerr Corporation

官方來源

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