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 |