The following data is part of a premarket notification filed by Alphatec Spine, Inc. with the FDA for Invictus™ Spinal Fixation System.
Device ID | K203056 |
510k Number | K203056 |
Device Name: | Invictus™ Spinal Fixation System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Alphatec Spine, Inc. 5818 E1 Camino Real Carlsbad, CA 92008 |
Contact | Cynthia Dorne |
Correspondent | Cynthia Dorne Alphatec Spine, Inc. 5818 E1 Camino Real Carlsbad, CA 92008 |
Product Code | NKB |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-10-08 |
Decision Date | 2020-11-23 |
Summary: | summary |