The following data is part of a premarket notification filed by Seaspine Orthopedics Corporation with the FDA for Seaspine® Daytona® Small Stature Spinal System.
| Device ID | K163604 |
| 510k Number | K163604 |
| Device Name: | SeaSpine® Daytona® Small Stature Spinal System |
| Classification | Thoracolumbosacral Pedicle Screw System |
| 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 | NKB |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-12-21 |
| Decision Date | 2017-03-09 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SEASPINE 86655624 4970455 Live/Registered |
SeaSpine, Inc. 2015-06-08 |
![]() SEASPINE 86459554 4919176 Live/Registered |
SeaSpine, Inc. 2014-11-20 |
![]() SEASPINE 76418251 2688666 Live/Registered |
SeaSpine, Inc. 2002-06-10 |