FDA 510(k), K021859, WRIST IMPLANT

FDA 510(k), K021859, WRIST IMPLANT

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510(K) Number: K021859
Device Name: WRIST IMPLANT
Manufacturer: AVANTA ORTHOPAEDICS, INC.
Device Classification Name: Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained
Regulation Number: 888.3800
Classification Product Code: JWJ
Date Received: 06/06/2002
Decision Date: 12/02/2002
Regulation Medical Specialty: Orthopedic

Total Pages: 73
Fully Redacted Pages: 48
Content Pages: 25
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