The following data is part of a premarket notification filed by Seaspine Orthopedics Corporation with the FDA for Seaspine Shoreline Acs - Anterior Cervical Standalone System.
Device ID | K161081 |
510k Number | K161081 |
Device Name: | SeaSpine Shoreline ACS - Anterior Cervical Standalone System |
Classification | Intervertebral Fusion Device With Integrated Fixation, Cervical |
Applicant | SEASPINE ORTHOPEDICS CORPORATION 5770 ARMADA DRIVE Carlsbad, CA 92008 |
Contact | Michelle Willis |
Correspondent | Jenny Fam SEASPINE ORTHOPEDICS CORPORATION 5770 ARMADA DRIVE Carlsbad, CA 92008 |
Product Code | OVE |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-04-18 |
Decision Date | 2016-09-14 |
Summary: | summary |