Otto Bock Healthcare Products GmbH
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2026-04-22
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K253256 | myosmart. (13E522); myosmart.cuff (757M20-2); connectgrip. (560X27-1); myosmart trial kit (642V64=T) | GXY | 2026-04-22 | View |
| 510(k) | K191179 | Myo Plus | GXY | 2019-09-04 | View |
No matching devices.