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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CONCORDE Bullet Lumbar Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
MODEL 3873 1* 8 AND MODEL 3874 1* 8 COMPACT TEST STIMULATION LEADS
FDA 510(k)
FDA Class 2
·Neurology
RENU MEDICAL REPROCESSED OXIMAX SENSORS: ADULT, PEDIATRIC, INFANT AND NEONATE
FDA 510(k)
FDA Class 2
·Cardiovascular
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar
Oximeter, Reprocessed
FDA classification
FDA Class 2
·Oximeter, Reprocessed
Stimulator, Spinal-Cord, Implanted (Pain Relief)
FDA classification
FDA Class 2
·Stimulator, Spinal-Cord, Implanted (Pain Relief)