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FDA 510(k), K946088, GENESIS POSTERIOR STABILIZED (P/S) KNEE SYSTEM
FDA 510(k), K946088, GENESIS POSTERIOR STABILIZED (P/S) KNEE SYSTEM
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510(K) Number: K946088
Device Name: GENESIS POSTERIOR STABILIZED (P/S) KNEE SYSTEM
Manufacturer: THOMAS L CRAIG
Device Classification Name: Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Regulation Number: JWH
Classification Product Code: KXA
Date Received: 12/13/1994
Decision Date: 08/08/1995
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: GENESIS POSTERIOR STABILIZED (P/S) KNEE SYSTEM
Manufacturer: THOMAS L CRAIG
Device Classification Name: Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Regulation Number: JWH
Classification Product Code: KXA
Date Received: 12/13/1994
Decision Date: 08/08/1995
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
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