FDA 510(k)

ORTHOLOC SPS 肩部固定系統

K 號：K181587 · 2018-10-05

決定日期2018-10-05

產品代碼HRS

諮詢委員會或

決定相當於

器材摘要

ORTHOLOC SPS Shoulder Plating System is the device name listed in this FDA 510(k) record. The listed applicant is Tornier, Inc.. It received FDA 510(k) clearance on 2018-10-05 under 510(k) number K181587. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ORTHOLOC SPS Shoulder Plating System?

ORTHOLOC SPS Shoulder Plating System is a medical device that received FDA 510(k) clearance on 2018-10-05. The listed applicant is Tornier, Inc.. The 510(k) number is K181587.

When did ORTHOLOC SPS Shoulder Plating System receive FDA 510(k) clearance?

ORTHOLOC SPS Shoulder Plating System received FDA 510(k) clearance on 2018-10-05, under 510(k) number K181587.

Who is the listed applicant for ORTHOLOC SPS Shoulder Plating System?

FDA 510(k) 記錄將 Tornier, Inc. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for ORTHOLOC SPS Shoulder Plating System?

The FDA product code for ORTHOLOC SPS Shoulder Plating System is HRS.

其他以 Tornier, 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。

K260721Tornier Perform 高級肩胛盂 K252788Tornier Perform™ 反向單柱盂蓋 (Perform Mono)K251686Tornier 臂骨重建系統 Max (Tornier HRS Max)K230352Tornier肩胛骨釘與Tornier長肩胛骨釘 K220914Tornier Perform 臂骨系統 – 骨折 K220418Tornier Perform 臂骨系統 – 齒冠式

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相關器械（代碼：HRS）

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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