The following data is part of a premarket notification filed by Seaspine Orthopedics Corporation with the FDA for Mariner Mis Pedicle Screw System; Seaspine Navigation System.
| Device ID | K191648 |
| 510k Number | K191648 |
| Device Name: | Mariner MIS Pedicle Screw System; SeaSpine Navigation System |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | SeaSpine Orthopedics Corporation 5770 Armada Drive Carlsbad, CA 92008 |
| Contact | Alicia Mcarthur |
| Correspondent | Aly Alvarez SeaSpine Orthopedics Corporation 5770 Armada Drive Carlsbad, CA 92008 |
| Product Code | NKB |
| Subsequent Product Code | KWQ |
| Subsequent Product Code | OLO |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-06-20 |
| Decision Date | 2019-07-19 |