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FDA 510(k), K892394, P.F.C. MODULAR KNEE SYSTEM, TIBIAL TRAY-POROUS
FDA 510(k), K892394, P.F.C. MODULAR KNEE SYSTEM, TIBIAL TRAY-POROUS
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510(K) Number: K892394
Device Name: P.F.C. MODULAR KNEE SYSTEM, TIBIAL TRAY-POROUS
Manufacturer: JOHNSON & JOHNSON PROFESSIONALS, INC.
Device Classification Name: prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer
Regulation Number: 888.3560
Classification Product Code: JWH
Date Received: 04/07/1989
Decision Date: 07/19/1989
Regulation Medical Specialty: Orthopedic
Device Name: P.F.C. MODULAR KNEE SYSTEM, TIBIAL TRAY-POROUS
Manufacturer: JOHNSON & JOHNSON PROFESSIONALS, INC.
Device Classification Name: prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer
Regulation Number: 888.3560
Classification Product Code: JWH
Date Received: 04/07/1989
Decision Date: 07/19/1989
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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