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 |