Autorizaciones FDA 510(k)
Dispositivos autorizados mediante 510(k) seguidos por MedTracker
IYE
2016-11-01
HRX
2016-11-01
AVAmax Vertebral Balloon, AVAflex Vertebral Balloon
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NDN
2016-11-01
13G InterV Kyphoplasty Catheter (Micro) and 11G InterV Kyphoplasty Catheter (Mini-Flex)
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HSD
2016-11-01
Anatomical Shoulder Domelock Dome centric
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MAX
2016-11-01
T-PAL Spacer System, T-PAL Titanium Spacer System, SYNFIX Evolution System
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JXI
2016-10-31
AxoGuard Nerve Connector
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LCJ
2016-10-31
Unger Quad Injector
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MSQ
2016-10-31
BreathID Hp Lab System
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DRS
2016-10-31
Disposable Pressure Transducer
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NEY
2016-10-31
miraDry System
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HRS
2016-10-31
Footmotion Plating System
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QEY
2016-10-31
Squirt Fluid Delivery System
Ver detalles →No hay dispositivos coincidentes.
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