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 |