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 |