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 |