OHI
2008-02-04
Orthosis, Foot Drop
FDA product code OHI · 1 cleared devices
Class 1
Physical Medicine
- Regulation
- 21 CFR 890.3475
- Review panel
- PM
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- Yes
- Clearance span
- 2008-02-04 – 2008-02-04
Aid for drop foot or similar disorders which have a lack of ankle dorsiflexion. Indicated for foot raising paresis.
No matching devices.
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