ClearanceBrief
510(k) K051948 ยท KRR Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer

AVON PATELLO-FEMORAL JOINT PROSTHESIS

ApplicantHowmedica Osteonics Corp., Mahwah NJ, US
DecisionSubstantially Equivalent, Oct 21, 2005
ReceivedJul 18, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K051948

DateFirm and productCodeLinked 510(k)
Sep 16, 2026Howmedica Osteonics Corp.
SCORPIO C-DOME PATELLA 73-2710 73-2910 SCORPIO U-DOME PATELLA 73-3110 73-3508 73-3708 73-3710 73-3910 Orthopaedic implant components manufactured from UHMWPE (polyethylene)
Open, Classified		 NPJNone listed
Jan 31, 2024Howmedica Osteonics Corp.
SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3110
Open, Classified		 JWHNone listed
Jan 31, 2024Howmedica Osteonics Corp.
SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3308
Open, Classified		 JWHNone listed
Jan 31, 2024Howmedica Osteonics Corp.
SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3508
Open, Classified		 JWHNone listed
Jan 31, 2024Howmedica Osteonics Corp.
SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3708
Open, Classified		 JWHNone listed
Jan 31, 2024Howmedica Osteonics Corp.
SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3710
Open, Classified		 JWHNone listed
Jan 31, 2024Howmedica Osteonics Corp.
Scorpio NRG Tibial Brg Insert Assy -Intended for knee replacement Part Number: 82-2-0910
Open, Classified		 JWHNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.