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 |