The following data is part of a premarket notification filed by Seaspine Orthopedics Corporation with the FDA for Shoreline Cervical Interbody Rt System.
Device ID | K183083 |
510k Number | K183083 |
Device Name: | Shoreline Cervical Interbody RT System |
Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
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 | ODP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-11-06 |
Decision Date | 2019-02-14 |
Summary: | summary |