FDA 510(k)

The Progressive Orthopaedic Total Hip System

Número K: K151424 · 2016-07-27

RequerenteThe Progressive Orthopaedic Company, LLC

Data da decisão2016-07-27

Código do produtoLPH

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

The Progressive Orthopaedic Total Hip System is the device name listed in this FDA 510(k) record. The listed applicant is The Progressive Orthopaedic Company, LLC. It received FDA 510(k) clearance on 2016-07-27 under 510(k) number K151424. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the The Progressive Orthopaedic Total Hip System?

The Progressive Orthopaedic Total Hip System is a medical device that received FDA 510(k) clearance on 2016-07-27. The listed applicant is The Progressive Orthopaedic Company, LLC. The 510(k) number is K151424.

When did The Progressive Orthopaedic Total Hip System receive FDA 510(k) clearance?

The Progressive Orthopaedic Total Hip System received FDA 510(k) clearance on 2016-07-27, under 510(k) number K151424.

Who is the listed applicant for The Progressive Orthopaedic Total Hip System?

The FDA 510(k) record lists The Progressive Orthopaedic Company, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for The Progressive Orthopaedic Total Hip System?

The FDA product code for The Progressive Orthopaedic Total Hip System is LPH.

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Fonte oficial

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