6 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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MODIFICATION TO OPTICAL TRACKING SYSTEM (OTS)
FDA 510(k)
FDA Class 2
·Neurology
M2376A DEVICELINK SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
MODULAR ROTATING HINGE KNEE CROSSOVER TIBIAL BEARING COMPONENTS
FDA 510(k)
FDA Class 2
·Orthopedic
Neurological Stereotaxic Instrument
FDA classification
FDA Class 2
·Neurological Stereotaxic Instrument
Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
FDA classification
FDA Class 2
·Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
FDA classification
FDA Class 2
·Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)