The following data is part of a premarket notification filed by Orthomedics with the FDA for Hip Abduction Splint.
| Device ID | K810557 |
| 510k Number | K810557 |
| Device Name: | HIP ABDUCTION SPLINT |
| Classification | Splint, Abduction, Congenital Hip Dislocation |
| Applicant | ORTHOMEDICS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IOZ |
| CFR Regulation Number | 890.3665 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-03-02 |
| Decision Date | 1981-03-13 |