6 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
×
AI.ME System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Powered Microneedle Device
FDA classification
FDA Class 2
·Powered Microneedle Device
Medtronic Model 5392 External Pulse Generator (EPG)
FDA 510(k)
FDA Class 2
·Cardiovascular
AMISTEM AND QUADRA - LINE EXTENSION
FDA 510(k)
FDA Class 2
·Orthopedic
Pulse-Generator, Pacemaker, External
FDA classification
FDA Class 2
·Pulse-Generator, Pacemaker, External
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
FDA classification
FDA Class 2
·Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented