The following data is part of a premarket notification filed by Choice Spine, Lp with the FDA for Tomcat Cervical Spinal System.
Device ID | K170953 |
510k Number | K170953 |
Device Name: | Tomcat Cervical Spinal System |
Classification | Intervertebral Fusion Device With Integrated Fixation, Cervical |
Applicant | Choice Spine, LP 400 Erin Drive Knoxville, TN 37919 |
Contact | Kim Finch |
Correspondent | Kim Finch Choice Spine, LP 400 Erin Drive Knoxville, TN 37919 |
Product Code | OVE |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-03-31 |
Decision Date | 2017-04-21 |
Summary: | summary |