79 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
FDA Pre-Market Approval
FDA Class 3
·LCS(R)TOTAL KNEE SYSTEM
Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
FDA Pre-Market Approval
FDA Class 3
·NEW JERSEY LCS(R) UNICOMPARTMENTAL KNEE
Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
FDA Pre-Market Approval
FDA Class 3
·LCS UNI KNEE SYSTEM
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT STRIP BONE GRAFT MATRIX
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·PRO OSTEON 500 BONE GRAFT SUBSTITUTE
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·PRO OSTEON 500 POROUS HYDROXYAPATITE BONE GRAFT SUBSTITUE BLOCKS & GRANULES
Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
FDA Pre-Market Approval
FDA Class 3
·NEW JERSEY LCS(R) UNICOMPARTMENTAL KNEE
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·PRO OSTEON IMPLANT 500 POROUS HYDROXYAPATITE BONE GRAFT SUBSTITUTE BLOCKS & GRANULES
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT(TM) BONE GRAFT MATRIX
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·NEUGRAFT
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·INTERPORE PRO OSTEAN(R)IMPLANT 500 COR. HYDROX
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·PRO OSTEON IMPLANT 500 CORALLINE HYDROXYPATITE BONE VOID FILLER (FORMERLY INTERPORE 500)
Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
FDA Pre-Market Approval
FDA Class 3
·LCS(R)TOTAL KNEE SYSTEM
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT(TM) BONE GRAFT SUBSTITUTE
Agent, Bulking, Injectable For Gastro-Urology Use
FDA Pre-Market Approval
FDA Class 3
·ENTERYX PROCEDURE KIT
Agent, Bulking, Injectable For Gastro-Urology Use
FDA Pre-Market Approval
FDA Class 3
·ENTERYX PROCEDURE KIT, MODEL M000572600
Agent, Bulking, Injectable For Gastro-Urology Use
FDA Pre-Market Approval
FDA Class 3
·ENTERYX PROCEDURE KIT
Agent, Bulking, Injectable For Gastro-Urology Use
FDA Pre-Market Approval
FDA Class 3
·ENTERYX PROCEDURE KIT
Agent, Bulking, Injectable For Gastro-Urology Use
FDA Pre-Market Approval
FDA Class 3
·ENTERYX PROCEDURE KIT