FDA 510(k)

Materialise 閃骨定位系統

K 號：K190286 · 2019-07-08

決定日期2019-07-08

產品代碼KWS

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決定相當於

器材摘要

Materialise Glenoid Positioning System is the device name listed in this FDA 510(k) record. The listed applicant is Materialise NV. It received FDA 510(k) clearance on 2019-07-08 under 510(k) number K190286. The device is classified under product code KWS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Materialise Glenoid Positioning System?

Materialise Glenoid Positioning System is a medical device that received FDA 510(k) clearance on 2019-07-08. The listed applicant is Materialise NV. The 510(k) number is K190286.

When did Materialise Glenoid Positioning System receive FDA 510(k) clearance?

Materialise Glenoid Positioning System received FDA 510(k) clearance on 2019-07-08, under 510(k) number K190286.

Who is the listed applicant for Materialise Glenoid Positioning System?

The FDA 510(k) record lists Materialise NV as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Materialise Glenoid Positioning System?

The FDA product code for Materialise Glenoid Positioning System is KWS.

其他以 Materialise NV 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。

K260802Materialise Shoulder System™，Materialise Shoulder Guide 及 Model，SurgiCase Shoulder Planner K251964模擬胸腔計劃器 K253308Materialise 頭顎面外科手術個人化導引和模型 CMF 鋼钛導引；CMF 塑膠模型 K253793Materialise 骨關節置换導引系統 K251554Materialise 骨關節置换導引系統 K243637Materialise個人化頭顱顏面手術導引和模型

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相關器械（代碼：KWS）

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Tornier, Inc.K254084AETOS肩關節系統 - CONCELOC關節盤Smith & Nephew, Inc.K252418催化劑F1x肩部系統Catalyst Orthoscience, Inc.K252416AETOS肩關節系統 Meta 肱骨假體尺寸 0Smith & Nephew, Inc.K241292MyShoulder Planner (5.3SSWPL)Medacta International S.A.K241878Tornier肩胛骨重建系統（Tornier HRS）；Tornier Perform肩胛骨系統 - 植骨（Tornier PHS-Stem）Stryker Corporation (Tornier, Inc.)

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