The following data is part of a premarket notification filed by Choice Spine, Lp with the FDA for Choice Spine Vertebral Body Replacement (vbr) Device System.
Device ID | K120570 |
510k Number | K120570 |
Device Name: | CHOICE SPINE VERTEBRAL BODY REPLACEMENT (VBR) DEVICE SYSTEM |
Classification | Spinal Vertebral Body Replacement Device |
Applicant | CHOICE SPINE, LP 400 Erin Dr Knoxville, TN 37919 |
Contact | Mark Bekkala |
Correspondent | Mark Bekkala CHOICE SPINE, LP 400 Erin Dr Knoxville, TN 37919 |
Product Code | MQP |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-02-27 |
Decision Date | 2012-04-05 |
Summary: | summary |