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Business · 05/03/2004

FDA Proposes New Requirements for Hip Joint Metal/Polymer or Ceramic/Polymer Semiconstrained Resurfacing Cemented Prosthesis

The Food and Drug Administration (FDA) is proposing to require manufacturers to submit a premarket approval application or a notice of completion of a product development protocol for a new type of hip joint prosthesis, citing concerns over potential risks and benefits to the public.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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