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FDA 510(k), K884796, P.F.C.(TM) MODULAR KNEE SYSTEM
FDA 510(k), K884796, P.F.C.(TM) MODULAR KNEE SYSTEM
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510(K) Number: K884796
Device Name: P.F.C.(TM) MODULAR KNEE SYSTEM
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: 11/16/1988
Decision Date: 03/29/1989
Regulation Medical Specialty: Orthopedic
Device Name: P.F.C.(TM) MODULAR KNEE SYSTEM
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: 11/16/1988
Decision Date: 03/29/1989
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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