84 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Pre Market Approval
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Bone Cement
FDA Pre-Market Approval
FDA Class 2
·PALACOS R BONE CEMENT
Bone Cement
FDA Pre-Market Approval
FDA Class 2
·PALACOS R BONE CEMENT
Bone Cement
FDA Pre-Market Approval
FDA Class 2
·PALACOS R BONE CEMENT
Bone Cement
FDA Pre-Market Approval
FDA Class 2
·OSTEOPAL
Bone Cement
FDA Pre-Market Approval
FDA Class 2
·PALACOS R BONE CEMENT
Bone Cement
FDA Pre-Market Approval
FDA Class 2
·PALACOS E-FLOW (OSTEOPAL) BONE CEMENT
Implanted Fecal Incontinence Device
FDA Pre-Market Approval
FDA Class 3
·AMS ACTICON NEOSPHINCTER
Somatic Gene Mutation Detection System
FDA Pre-Market Approval
FDA Class 3
·COBAS 4800 BRAF V600 MUTATION TEST
Somatic Gene Mutation Detection System
FDA Pre-Market Approval
FDA Class 3
·cobas® BRAF V600 Mutation Test
Implanted Fecal Incontinence Device
FDA Pre-Market Approval
FDA Class 3
·ACTICON NEOSPHINCTER ARTIFICAL BOWEL SPHINCTER
Somatic Gene Mutation Detection System
FDA Pre-Market Approval
FDA Class 3
·Roche cobas DNA Sample Preparation Kit / Roche cobas 4800 BRAF V600 Mutation Test
Somatic Gene Mutation Detection System
FDA Pre-Market Approval
FDA Class 3
·cobas BRAF V600 Mutation Test
Implanted Fecal Incontinence Device
FDA Pre-Market Approval
FDA Class 3
·ACTICON NEOSPHINCTER
Implanted Fecal Incontinence Device
FDA Pre-Market Approval
FDA Class 3
·AMS ACTICON NEOSPHINCTER ARTIFICIAL BOWEL SPHINCTER (ABS)
Implanted Fecal Incontinence Device
FDA Pre-Market Approval
FDA Class 3
·ACTICON NEOSPHINCTER ARTIFICIAL BOWEL SPHINCTER
Implanted Fecal Incontinence Device
FDA Pre-Market Approval
FDA Class 3
·ACTICON NEOSPHINCTER
Implanted Fecal Incontinence Device
FDA Pre-Market Approval
FDA Class 3
·AMS ACTICON NEOSPHINCTER
Somatic Gene Mutation Detection System
FDA Pre-Market Approval
FDA Class 3
·COBAS 4800 BRAF V600 MUTATION TEST
Implanted Fecal Incontinence Device
FDA Pre-Market Approval
FDA Class 3
·AMS ACTICON NEOSPHINCTER- ARTIFICIAL BOWL SPHINCTER (ABS)
Somatic Gene Mutation Detection System
FDA Pre-Market Approval
FDA Class 3
·cobas® 4800 BRAF V600 Mutation Test