The following data is part of a premarket notification filed by Hosmer Dorrance Corp. with the FDA for Post-operative Hip Orthosis.
| Device ID | K780891 |
| 510k Number | K780891 |
| Device Name: | POST-OPERATIVE HIP ORTHOSIS |
| Classification | Joint, Hip, External Brace |
| Applicant | HOSMER DORRANCE CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | ITS |
| CFR Regulation Number | 890.3475 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-05-31 |
| Decision Date | 1978-06-13 |