49 results
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17ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT BONE GRAFT MATRIX
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·INTERPORE PRO OSTEON IMPLANT 500 CORALLINE HYDROXYAPATITE BONE VOID FILLER
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT(TM) BONE GRAFT SUBSTITUTE
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
·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
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)
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT(TM) BONE GRAFT SUBSTITUTE
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing
FDA Pre-Market Approval
FDA Class 3
·LCS Total Knee System
Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-Constrained, Metal/Polymer, Mobile Bearing
FDA Pre-Market Approval
FDA Class 3
·OXFORD PARTIAL KNEE
Lymph Node Location System During Sentinel Biopsy Procedure
FDA Pre-Market Approval
FDA Class 3
·Magtrace/and Sentimag Magnetic Localization System
Lymph Node Location System During Sentinel Biopsy Procedure
FDA Pre-Market Approval
FDA Class 3
·Magtrace and Sentimag Magnetic Localization System
Lymph Node Location System During Sentinel Biopsy Procedure
FDA Pre-Market Approval
FDA Class 3
·MagtraceTM and Sentimag(R) Magnetic Locatization System
Lymph Node Location System During Sentinel Biopsy Procedure
FDA Pre-Market Approval
FDA Class 3
·MagtraceTM and Sentimag(R) Magnetic Locatization System
Lymph Node Location System During Sentinel Biopsy Procedure
FDA Pre-Market Approval
FDA Class 3
·MagtraceTM and Sentimag(R) Magnetic Locatization System