The following data is part of a premarket notification filed by Lanx, Inc. with the FDA for Lanx Lateral.
| Device ID | K103666 |
| 510k Number | K103666 |
| Device Name: | LANX LATERAL |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | LANX, INC. 390 INTERLOCKEN CRESCENT SUITE 890 Broomfield, CO 80021 |
| Contact | Alan Brukholder |
| Correspondent | Alan Brukholder LANX, INC. 390 INTERLOCKEN CRESCENT SUITE 890 Broomfield, CO 80021 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-12-15 |
| Decision Date | 2011-03-23 |
| Summary: | summary |