The following data is part of a premarket notification filed by Vgi, Llc with the FDA for Vertelp Interbody Fusion Device.
| Device ID | K151312 |
| 510k Number | K151312 |
| Device Name: | VerteLP Interbody Fusion Device |
| Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
| Applicant | VGI, LLC 150 253rd Ave St. Petersburg, FL 33708 |
| Contact | Tov Vestgaarten |
| Correspondent | Rich Jansen Silver Pine Consulting, LLC. 11821 Bramble Cove Drive Ft. Myers, FL 33905 |
| Product Code | OVD |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-05-18 |
| Decision Date | 2016-01-13 |
| Summary: | summary |