REDAPT Anteverted Cemented Liner — FDA 510(k) K160923

医療機器の概要

REDAPT Anteverted Cemented Liner is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2016-11-17 under 510(k) number K160923. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the REDAPT Anteverted Cemented Liner?

REDAPT Anteverted Cemented Liner is a medical device that received FDA 510(k) clearance on 2016-11-17. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K160923.

When did REDAPT Anteverted Cemented Liner receive FDA 510(k) clearance?

REDAPT Anteverted Cemented Liner received FDA 510(k) clearance on 2016-11-17, under 510(k) number K160923.

Who is the listed applicant for REDAPT Anteverted Cemented Liner?

The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REDAPT Anteverted Cemented Liner?

The FDA product code for REDAPT Anteverted Cemented Liner is JDI.

申請者としてSmith & Nephew, Inc.を記載するその他の記録

関連レコードは、名称、製品コード、その他のメタデータを使用して自動的にマッチングされます。マッチは検証された臨床的、科学的、企業的、または規制上の関係を確立するものではありません。リンクされた公式情報源をご確認ください。

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関連機器（コード：JDI）

関連レコードは、名称、製品コード、その他のメタデータを使用して自動的にマッチングされます。マッチは検証された臨床的、科学的、企業的、または規制上の関係を確立するものではありません。リンクされた公式情報源をご確認ください。

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