FDA 510(k)

內部干擾 - 無菌

K 號：K161470 · 2016-12-01

決定日期2016-12-01

產品代碼MQN

諮詢委員會DE

決定相當於

器材摘要

Internal Distraction - Sterile is the device name listed in this FDA 510(k) record. The listed applicant is KLS Martin L.P.. It received FDA 510(k) clearance on 2016-12-01 under 510(k) number K161470. The device is classified under product code MQN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Internal Distraction - Sterile?

Internal Distraction - Sterile is a medical device that received FDA 510(k) clearance on 2016-12-01. The listed applicant is KLS Martin L.P.. The 510(k) number is K161470.

When did Internal Distraction - Sterile receive FDA 510(k) clearance?

Internal Distraction - Sterile received FDA 510(k) clearance on 2016-12-01, under 510(k) number K161470.

Who is the listed applicant for Internal Distraction - Sterile?

The FDA 510(k) record lists KLS Martin L.P. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Internal Distraction - Sterile?

The FDA product code for Internal Distraction - Sterile is MQN.

其他以 KLS Martin L.P. 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。

K260137KLS Martin IPS 口腔-馬克斯植入物 - MR條件性；個人患者解決方案 - Ti (IPS-Ti)；個人患者解決方案 - PEEK (IPS-PEEK)；KLS Martin 個人患者解決方案 K254162KLS Martin Ixos 系統 K253660KLS Martin 純淨胸骨系統 K250988KLS Martin 純淨胸骨系統 K250865KLS Martin IPS 臂部系統 K252573KLS Martin 頭蓋內植物 - MR條件性；K944565：KLS-Martin 微骨固定系統（1.5MM）；K971297：KLS Martin 中心驅動無釘螺釘；K060177：KLS Martin 嚴格固定 - 無菌；K062570：個人化病人解決方案 - Ti（IPS-Ti）；K072707：個人化病人解決方案 - PEEK（IPS-PEEK）；K151382：個人化病人解決方案 - （IPS-PEEK）- 無菌

查看所有 33 項裝置 →

相關器械（代碼：MQN）

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。

K220050KLS Martin IPS 分離器KLS Martin L.P.K183113DePuy Synthes 頭顎外科產品系列 - MR條件性Synthes (USA) Products, LLC K181504Stryker兒童顎骨分離器2Stryker K162594頭顱顎面骨擴張系統 (CMFD)Synthes USA Products, LLC

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。