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FDA 510(k) K122158, PBP TOTAL HIP SYSTEM, by Pipeline Biomedical Products, LLC

FDA 510(k) K122158, PBP TOTAL HIP SYSTEM, by Pipeline Biomedical Products, LLC

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510(K) Number: K122158
Device Name: PBP TOTAL HIP SYSTEM
Manufacturer: Pipeline Biomedical Products, LLC
Device Classification Name: hip prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented
Regulation Number: 888.3358
Classification Product Code: OQG
Date Received: 07/20/2012
Decision Date: 12/11/2012
Regulation Medical Specialty: Orthopedic
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