FDA 510(k)

NIM PAK針；NIM XPAK針；NIM骨針探針

K 號：K180542 · 2018-08-22

決定日期2018-08-22

產品代碼PDQ

諮詢委員會中文(台灣): 此醫療設備之規範性文件遵循「醫療規範-v1」政策。以下為該文件之翻譯：此醫療設備已通過美國食品藥品管理局（FDA）的510(k)認證，並獲得PMA許可。該設備的臨床試驗編號為NCTXXXXXXX，並在PubMed上以PMIDXXXXXXX登錄。該設備的識別碼為XXXXXXXX，相關資訊請參考以下網址：[URL]。公司名稱：[公司名稱] 產品名稱：[產品名稱]

決定相當於

器材摘要

NIM PAK Needle; NIM XPAK Needle; NIM Pedicle Probe is the device name listed in this FDA 510(k) record. The listed applicant is Boston Endo Surgical Tech,. It received FDA 510(k) clearance on 2018-08-22 under 510(k) number K180542. The device is classified under product code PDQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the NIM PAK Needle; NIM XPAK Needle; NIM Pedicle Probe?

NIM PAK Needle; NIM XPAK Needle; NIM Pedicle Probe is a medical device that received FDA 510(k) clearance on 2018-08-22. The listed applicant is Boston Endo Surgical Tech,. The 510(k) number is K180542.

When did NIM PAK Needle; NIM XPAK Needle; NIM Pedicle Probe receive FDA 510(k) clearance?

NIM PAK Needle; NIM XPAK Needle; NIM Pedicle Probe received FDA 510(k) clearance on 2018-08-22, under 510(k) number K180542.

Who is the listed applicant for NIM PAK Needle; NIM XPAK Needle; NIM Pedicle Probe?

The FDA 510(k) record lists Boston Endo Surgical Tech, as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NIM PAK Needle; NIM XPAK Needle; NIM Pedicle Probe?

The FDA product code for NIM PAK Needle; NIM XPAK Needle; NIM Pedicle Probe is PDQ.

其他以 Boston Endo Surgical Tech, 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。

K182662NAV PAK針筒，NIM NAV PAK針筒

相關器械（代碼：PDQ）

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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官方來源

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