The following data is part of a premarket notification filed by Medi-ked, Inc. with the FDA for Kendrick Extrication Device.
| Device ID | K781761 |
| 510k Number | K781761 |
| Device Name: | KENDRICK EXTRICATION DEVICE |
| Classification | Orthosis, Cervical-thoracic, Rigid |
| Applicant | MEDI-KED, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IQF |
| CFR Regulation Number | 890.3490 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-10-16 |
| Decision Date | 1978-10-27 |