The following data is part of a premarket notification filed by Seaspine Orthopedics Corporation with the FDA for Seaspine Regatta Lateral System.
Device ID | K181079 |
510k Number | K181079 |
Device Name: | SeaSpine Regatta Lateral System |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
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 | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-04-24 |
Decision Date | 2018-07-18 |
Summary: | summary |