FDA 510(k), K951987, GENESIS II TOTAL KNEE SYSTEM

FDA 510(k), K951987, GENESIS II TOTAL KNEE SYSTEM

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510(K) Number: K951987
Device Name: GENESIS II TOTAL KNEE SYSTEM
Manufacturer: THOMAS L CRAIG
Device Classification Name: Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Regulation Number: JWH
Classification Product Code: 04/27/1995
Date Received: 08/22/1995
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic

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