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FDA 510(k), K032163, DURACON TOTAL KNEE SYSTEM
FDA 510(k), K032163, DURACON TOTAL KNEE SYSTEM
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$149.00 USD
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$149.00 USD
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510(K) Number: K032163
Device Name: DURACON TOTAL KNEE SYSTEM
Manufacturer:
Device Classification Name: Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Regulation Number: 888.3565
Classification Product Code: MBH
Date Received: 07/15/2003
Decision Date: 09/12/2003
Regulation Medical Specialty: Orthopedic
Device Name: DURACON TOTAL KNEE SYSTEM
Manufacturer:
Device Classification Name: Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Regulation Number: 888.3565
Classification Product Code: MBH
Date Received: 07/15/2003
Decision Date: 09/12/2003
Regulation Medical Specialty: Orthopedic
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