The following data is part of a premarket notification filed by Choice Spine, Lp with the FDA for Choice Spine Fixation System.
Device ID | K121850 |
510k Number | K121850 |
Device Name: | CHOICE SPINE FIXATION SYSTEM |
Classification | System, Facet Screw Spinal Device |
Applicant | CHOICE SPINE, LP 400 Erin Dr Knoxville, TN 37919 |
Contact | Kim Finch |
Correspondent | Kim Finch CHOICE SPINE, LP 400 Erin Dr Knoxville, TN 37919 |
Product Code | MRW |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-06-25 |
Decision Date | 2012-09-20 |
Summary: | summary |