The following data is part of a premarket notification filed by Choice Spine, Lp with the FDA for Choice Spine Lumbar Spacer System (sabre™, Shark™, Hornet™, Harpoon™), Choice Spine Veo™ Lateral Access & Interbody Fusion System, Choice Spine Interbody Fusion System.
Device ID | K153107 |
510k Number | K153107 |
Device Name: | Choice Spine Lumbar Spacer System (Sabre™, Shark™, Hornet™, Harpoon™), Choice Spine VEO™ Lateral Access & Interbody Fusion System, Choice Spine Interbody Fusion 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 | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-10-27 |
Decision Date | 2016-05-19 |
Summary: | summary |