The following data is part of a premarket notification filed by Choice Spine with the FDA for Thunderbolt™ Minimally Invasive And Lancer™ Open Pedicle Screw Systems.
Device ID | K171456 |
510k Number | K171456 |
Device Name: | Thunderbolt™ Minimally Invasive And Lancer™ Open Pedicle Screw Systems |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Choice Spine 400 Erin Drive Knoxville, TN 37919 |
Contact | Kim Finch |
Correspondent | Kim Finch Choice Spine 400 Erin Drive Knoxville, TN 37919 |
Product Code | NKB |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-05-17 |
Decision Date | 2017-08-03 |
Summary: | summary |