549 results
·
19ms
·
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
·NATURAL-KNEE(R) AND NATURAL KNEE(R)II W/CSTI(TM)
Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
FDA Pre-Market Approval
FDA Class 3
·LCS UNICOMPARTMENTAL KNEE SYSTEM
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA ARTIFICIAL SKIN DERMAL REGENERATION TEMPLATE
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA DERMAL REGENERATION TEMPLATE
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·GAMBRO AB PLASMAFILTER PF 2000N AND EXCORIM KB MAXO PLASMAFILTER
Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
FDA Pre-Market Approval
FDA Class 3
·NATURAL KNEE & NATURAL KNEE II
Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
FDA Pre-Market Approval
FDA Class 3
·LCS(R)TOTAL KNEE SYSTEM
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA ARTIFICIAL SKIN REGENERATION TEMPLATE
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA DERMAL REGENERATION TEMPLATE
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·Plasmaflo OP-05W(A)
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·GAMBRO PRISM TPE 2000 SET WITH PLASMAFILTER PF2000N
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·DERMAL REGENERATION TEMPLATE
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·Prismaflex TPE2000 Set
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·Gambro Prismaflex TPE 2000 Set
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA DERMAL REGENERATION TEMPLATE
Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
FDA Pre-Market Approval
FDA Class 3
·NEW JERSEY LCS(R) UNICOMPARTMENTAL KNEE
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA DERMAL REGENERATION TEMPLATE
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·GAMBRO PRISMAFLEX TPE 2000 SET
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA DERMAL REGENERATION TEMPLATE
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·PROSORBA(TM) COLUMN