FDA 510(k)

Stryker Orthopaedics Hip Systems Labeling Update

K-번호: K153345 · 2016-05-25

결정일2016-05-25

제품 코드LPH

자문 위원회OR

결정Substantially Equivalent

기기 요약

Stryker Orthopaedics Hip Systems Labeling Update is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Orthopaedics. It received FDA 510(k) clearance on 2016-05-25 under 510(k) number K153345. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Stryker Orthopaedics Hip Systems Labeling Update?

Stryker Orthopaedics Hip Systems Labeling Update is a medical device that received FDA 510(k) clearance on 2016-05-25. The listed applicant is Stryker Orthopaedics. The 510(k) number is K153345.

When did Stryker Orthopaedics Hip Systems Labeling Update receive FDA 510(k) clearance?

Stryker Orthopaedics Hip Systems Labeling Update received FDA 510(k) clearance on 2016-05-25, under 510(k) number K153345.

Who is the listed applicant for Stryker Orthopaedics Hip Systems Labeling Update?

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

What is the FDA product code for Stryker Orthopaedics Hip Systems Labeling Update?

The FDA product code for Stryker Orthopaedics Hip Systems Labeling Update is LPH.

Stryker Orthopaedics를 신청인으로 등재한 기타 기록

K211703Insignia Hip Stem K191414EXETER Centralizer, EXETER 2.5mm Plug K173499Exeter V40 Femoral Stem Hip System, Orthinox V40 Femoral Heads K173849Triathlon Total Knee System K172326Triathlon Total Knee System, Triathlon PKR System, Restoris MCK Knee System

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