The following data is part of a premarket notification filed by Orthofix, Inc. with the FDA for Centurion Poct System.
| Device ID | K150822 |
| 510k Number | K150822 |
| Device Name: | Centurion POCT System |
| Classification | Posterior Cervical Screw System |
| Applicant | ORTHOFIX, INC. 3451 PLANO PARKWAY Lewisville, TX 75056 |
| Contact | Jacki Geren |
| Correspondent | Jacki Geren ORTHOFIX, INC. 3451 PLANO PARKWAY Lewisville, TX 75056 |
| Product Code | NKG |
| CFR Regulation Number | 888.3075 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-03-27 |
| Decision Date | 2015-05-15 |
| Summary: | summary |