FDA 510(k), K003269, UNICONDYLAR INTERPOSITIONAL SPACER

FDA 510(k), K003269, UNICONDYLAR INTERPOSITIONAL SPACER

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510(K) Number: K003269
Device Name: UNICONDYLAR INTERPOSITIONAL SPACER
Manufacturer:
Device Classification Name: Prosthesis, Knee, Hemi-, Tibial, Resurfacing (Uncemented)
Regulation Number: 888.3590
Classification Product Code: HSH
Date Received: 10/18/2000
Decision Date: 01/04/2001
Regulation Medical Specialty: Orthopedic
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