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 |