The following data is part of a premarket notification filed by Choice Spine, Lp with the FDA for Choicespine™ Proliant® Posterior Pedicle Screw And Hook Fixation System.
| Device ID | K170821 |
| 510k Number | K170821 |
| Device Name: | ChoiceSpine™ Proliant® Posterior Pedicle Screw And Hook Fixation System |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | Choice Spine, LP 400 Erin Drive Knoxville, TN 37919 |
| Contact | Kim Finch |
| Correspondent | Jim Banic Exactech Inc 2320 NW 66th Court Gainesville, FL 32653 |
| Product Code | NKB |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-03-20 |
| Decision Date | 2017-06-08 |
| Summary: | summary |