The following data is part of a premarket notification filed by Curiteva, Inc. with the FDA for Curiteva Pedicle Screw System.
| Device ID | K191810 |
| 510k Number | K191810 |
| Device Name: | Curiteva Pedicle Screw System |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | Curiteva, Inc. 25127 Will McComb Drive Tanner, AL 35671 |
| Contact | Eric Linder |
| Correspondent | Eric Linder Curiteva, Inc. 25127 Will McComb Drive Tanner, AL 35671 |
| Product Code | NKB |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-07-05 |
| Decision Date | 2019-08-28 |