The following data is part of a premarket notification filed by Choice Spine, Lp with the FDA for Harrier-sa™ Lumbar Interbody System.
Device ID | K180519 |
510k Number | K180519 |
Device Name: | HARRIER-SA™ Lumbar Interbody System |
Classification | Intervertebral Fusion Device With Integrated Fixation, 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 | OVD |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-02-27 |
Decision Date | 2018-05-16 |
Summary: | summary |