The following data is part of a premarket notification filed by Choice Spine with the FDA for Choice Spine Hawkeye™ Vertebral Body Replacement (vbr) System.
Device ID | K171686 |
510k Number | K171686 |
Device Name: | Choice Spine Hawkeye™ Vertebral Body Replacement (VBR) System |
Classification | Spinal Vertebral Body Replacement Device |
Applicant | Choice Spine 400 Erin Drive Knoxville, TN 37924 |
Contact | Kim Finch |
Correspondent | Kim Finch Choice Spine 400 Erin Drive Knoxville, TN 37924 |
Product Code | MQP |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-06-07 |
Decision Date | 2017-09-15 |
Summary: | summary |