The following data is part of a premarket notification filed by Seaspine Orthopedics Corporation with the FDA for Seaspine Cabo Acp (anterior Cervical Plate) System.
Device ID | K173521 |
510k Number | K173521 |
Device Name: | SeaSpine Cabo ACP (Anterior Cervical Plate) System |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | SeaSpine Orthopedics Corporation 5770 Armada Drive Carlsbad, CA 92008 |
Contact | Gina Flores |
Correspondent | Gina Flores SeaSpine Orthopedics Corporation 5770 Armada Drive Carlsbad, CA 92008 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-11-14 |
Decision Date | 2018-01-24 |
Summary: | summary |