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).
Device ID | K140142 |
510k Number | K140142 |
Device Name: | CHOICE SPINE LUMBAR SPACER SYSTEM (SABRE, SHARK, HORNET, HARPOON) |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | CHOICE SPINE, LP 306 ERIN DRIVE Knoxville, TN 37919 -2141 |
Contact | Kim Finch |
Correspondent | Kim Finch CHOICE SPINE, LP 306 ERIN DRIVE Knoxville, TN 37919 -2141 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-01-22 |
Decision Date | 2014-07-16 |
Summary: | summary |