The following data is part of a premarket notification filed by Precision Spine with the FDA for Nexgen Anterior Cervical Plate System.
| Device ID | K192494 |
| 510k Number | K192494 |
| Device Name: | NexGen Anterior Cervical Plate System |
| Classification | Appliance, Fixation, Spinal Intervertebral Body |
| Applicant | Precision Spine 2050 Executive Drive Pearl, MS 39208 |
| Contact | Michael C. Dawson |
| Correspondent | J. D. Webb The OrthoMedix Group, Inc. 4313 W. 3800 S. West Haven, UT 84401 |
| Product Code | KWQ |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-09-11 |
| Decision Date | 2019-10-29 |
| Summary: | summary |