The following data is part of a premarket notification filed by Choice Spine, Lp with the FDA for Blackbird Spinal System.
Device ID | K133214 |
510k Number | K133214 |
Device Name: | BLACKBIRD SPINAL SYSTEM |
Classification | Appliance, Fixation, Spinal Interlaminal |
Applicant | CHOICE SPINE, LP 400 Erin Dr Knoxville, TN 37919 |
Contact | Kim Finch |
Correspondent | Kim Finch CHOICE SPINE, LP 400 Erin Dr Knoxville, TN 37919 |
Product Code | KWP |
CFR Regulation Number | 888.3050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-10-18 |
Decision Date | 2014-03-07 |
Summary: | summary |