The following data is part of a premarket notification filed by Fred Sammons, Inc. with the FDA for Obthoses.
| Device ID | K821641 |
| 510k Number | K821641 |
| Device Name: | OBTHOSES |
| Classification | Orthosis, Limb Brace |
| Applicant | FRED SAMMONS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IQI |
| CFR Regulation Number | 890.3475 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-06-03 |
| Decision Date | 1982-06-11 |