The following data is part of a premarket notification filed by Evolution Spine, Llc with the FDA for Whistler Modular Pedicle Screw System.
Device ID | K182478 |
510k Number | K182478 |
Device Name: | Whistler Modular Pedicle Screw System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Evolution Spine, LLC 4225 Office Parkway Dallas, TX 75204 |
Contact | Douglas Davis |
Correspondent | Douglas Davis Evolution Spine, LLC 4225 Office Parkway Dallas, TX 75204 |
Product Code | NKB |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-09-10 |
Decision Date | 2019-01-15 |
Summary: | summary |