The following data is part of a premarket notification filed by Ldr Spine Usa, Inc. with the FDA for Vertefit Corpectomy Cage System.
Device ID | K162133 |
510k Number | K162133 |
Device Name: | VerteFIT Corpectomy Cage System |
Classification | Spinal Vertebral Body Replacement Device |
Applicant | LDR SPINE USA, INC. 13785 RESEARCH BLVD SUITE 200 Austin, TX 78750 |
Contact | Jamie Wilson |
Correspondent | Bradley W Strasser LDR SPINE USA, INC. 13785 RESEARCH BLVD SUITE 200 Austin, TX 78750 |
Product Code | MQP |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-08-01 |
Decision Date | 2017-05-16 |
Summary: | summary |