Townsend Design
3 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 1 recall (Z-0670-2024) | Townsend Design | 2024-01-05 |
| SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: recall (Z-0671-2024) | Townsend Design | 2024-01-05 |
| SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, R recall (Z-0672-2024) | Townsend Design | 2024-01-05 |
Track Townsend Design automatically
Every clearance here is in the API, with alerts when new ones post.