The following data is part of a premarket notification filed by Ldr Spine Usa Inc. with the FDA for Ldr Spine Usa Avenue L Interbody Fusion.
| Device ID | K113285 |
| 510k Number | K113285 |
| Device Name: | LDR SPINE USA AVENUE L INTERBODY FUSION |
| Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
| Applicant | LDR SPINE USA INC. 13785 RESEARCH BOULEVARD SUITE 200 Austin, TX 78750 |
| Contact | Maritza Elias |
| Correspondent | Maritza Elias LDR SPINE USA INC. 13785 RESEARCH BOULEVARD SUITE 200 Austin, TX 78750 |
| Product Code | OVD |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-11-07 |
| Decision Date | 2012-07-26 |
| Summary: | summary |