The following data is part of a premarket notification filed by Seaspine Orthopedics Corporation with the FDA for Seaspine Meridian System, Seaspine Meridian Anterior Plate System.
Device ID | K220711 |
510k Number | K220711 |
Device Name: | SeaSpine Meridian System, SeaSpine Meridian Anterior Plate System |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | SeaSpine Orthopedics Corporation 5770 Armada Drive Carlsbad, CA 92008 |
Contact | Kavita Chandrashekar |
Correspondent | Jesse Albright SeaSpine Orthopedics Corporation 5770 Armada Drive Carlsbad, CA 92008 |
Product Code | MAX |
Subsequent Product Code | KWQ |
Subsequent Product Code | OVD |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2022-03-11 |
Decision Date | 2022-05-10 |