Medical Device Manufacturer · AT , Vienna

Otto Bock Healthcare Products GmbH - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2015

Recent clearances: myosmart. (13E522), Myo Plus, MYGAIT STIMULATION SYSTEM

View 3 510(k) Devices ↓
3
Total
3
Cleared
0
Denied

FDA 510(k) Regulatory Record - Otto Bock Healthcare Products GmbH Neurology ✕

3 devices
1-3 of 3
Cleared Apr 22, 2026
myosmart. (13E522)
K253256 · GXY
Neurology · 205d
Cleared Sep 04, 2019
Myo Plus
K191179 · GXY
Neurology · 125d
Cleared Apr 02, 2015
MYGAIT STIMULATION SYSTEM
K141812 · GZI
Neurology · 269d
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