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FDA 510(k), K011533, DEPUY FEMORAL HEADS
FDA 510(k), K011533, DEPUY FEMORAL HEADS
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510(K) Number: K011533
Device Name: DEPUY FEMORAL HEADS
Manufacturer: DEPUY ORTHOPAEDICS, INC.
Device Classification Name: Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Regulation Number: 888.3353
Classification Product Code: LZO
Date Received: 05/18/2001
Decision Date: 01/28/2002
Regulation Medical Specialty: Orthopedic
Device Name: DEPUY FEMORAL HEADS
Manufacturer: DEPUY ORTHOPAEDICS, INC.
Device Classification Name: Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Regulation Number: 888.3353
Classification Product Code: LZO
Date Received: 05/18/2001
Decision Date: 01/28/2002
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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