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 |