The following data is part of a premarket notification filed by Lanx, Inc. with the FDA for Lanx Spinal Fization System.
| Device ID | K121316 |
| 510k Number | K121316 |
| Device Name: | LANX SPINAL FIZATION SYSTEM |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | LANX, INC. 310 INTERLOCKEN PARKWAY SUITE 120 Broomfield, CO 80021 |
| Contact | William Sandul |
| Correspondent | William Sandul LANX, INC. 310 INTERLOCKEN PARKWAY SUITE 120 Broomfield, CO 80021 |
| 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 | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-05-02 |
| Decision Date | 2012-09-10 |
| Summary: | summary |