The following data is part of a premarket notification filed by Nuvasive, Inc. with the FDA for Nuvasive Spherx Ii -mas Deformity Spinal System.
| Device ID | K102514 |
| 510k Number | K102514 |
| Device Name: | NUVASIVE SPHERX II -MAS DEFORMITY SPINAL SYSTEM |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | NUVASIVE, INC. 7475 LUSK BLVD San Diego, CA 92121 |
| Contact | Elisa Ketchum |
| Correspondent | Elisa Ketchum NUVASIVE, INC. 7475 LUSK BLVD San Diego, CA 92121 |
| Product Code | NKB |
| Subsequent Product Code | KWP |
| Subsequent Product Code | KWQ |
| 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 | 2010-09-01 |
| Decision Date | 2010-12-01 |
| Summary: | summary |