FDA 510(k), K112174, NCB PERIPROSTHETIC FEMUR POLYAXIAL LOCKING PLATE SYSTEM

FDA 510(k), K112174, NCB PERIPROSTHETIC FEMUR POLYAXIAL LOCKING PLATE SYSTEM

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510(K) Number: K112174
Device Name: NCB PERIPROSTHETIC FEMUR POLYAXIAL LOCKING PLATE SYSTEM
Manufacturer: ZIMMER, INC.
Device Classification Name: plate, fixation, bone
Regulation Number: 888.3030
Classification Product Code: HRS
Date Received: 07/28/2011
Decision Date: 10/26/2011
Regulation Medical Specialty: Orthopedic
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