The following data is part of a premarket notification filed by Choice Spine, Lp. with the FDA for Tiger Shark™ System.
Device ID | K172816 |
510k Number | K172816 |
Device Name: | TiGer Shark™ System |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
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 | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-09-18 |
Decision Date | 2018-01-26 |
Summary: | summary |