The following data is part of a premarket notification filed by Seaspine, Inc. with the FDA for Malibu Spinal System With The Daytona Deformity System.
| Device ID | K122571 |
| 510k Number | K122571 |
| Device Name: | MALIBU SPINAL SYSTEM WITH THE DAYTONA DEFORMITY SYSTEM |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | SEASPINE, INC. 2302 La Mirada Dr Vista, CA 92081 |
| Contact | Ethel Bernal |
| Correspondent | Ethel Bernal SEASPINE, INC. 2302 La Mirada Dr Vista, CA 92081 |
| Product Code | NKB |
| Subsequent Product Code | KWP |
| Subsequent Product Code | MNH |
| Subsequent Product Code | MNI |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-08-23 |
| Decision Date | 2012-12-12 |
| Summary: | summary |