FDA 510(k), K073102, BIOLOX DELTA CERAMIC HEADS WITH 100KGY E-POLY ACETABULAR LINERS
FDA 510(k), K073102, BIOLOX DELTA CERAMIC HEADS WITH 100KGY E-POLY ACETABULAR LINERS
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510(K) Number: K073102
Device Name: BIOLOX DELTA CERAMIC HEADS WITH 100KGY E-POLY ACETABULAR LINERS
Manufacturer:
Device Classification Name: Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Regulation Number: 888.3353
Classification Product Code: LZO
Date Received: 11/02/2007
Decision Date: 11/27/2007
Regulation Medical Specialty: Orthopedic
Device Name: BIOLOX DELTA CERAMIC HEADS WITH 100KGY E-POLY ACETABULAR LINERS
Manufacturer:
Device Classification Name: Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Regulation Number: 888.3353
Classification Product Code: LZO
Date Received: 11/02/2007
Decision Date: 11/27/2007
Regulation Medical Specialty: Orthopedic