The following data is part of a premarket notification filed by Spinal Elements, Inc. with the FDA for Lucent Magnum+.
| Device ID | K081711 |
| 510k Number | K081711 |
| Device Name: | LUCENT MAGNUM+ |
| Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
| Applicant | SPINAL ELEMENTS, INC. 2744 LOKER AVE. W. SUITE 100 Carlsbad, CA 92008 |
| Contact | Kerri Dimartino |
| Correspondent | Kerri Dimartino SPINAL ELEMENTS, INC. 2744 LOKER AVE. W. SUITE 100 Carlsbad, CA 92008 |
| Product Code | OVD |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-06-17 |
| Decision Date | 2008-09-11 |
| Summary: | summary |