The following data is part of a premarket notification filed by Seaspine Orthopedics Corporation with the FDA for Seaspine® Vu A•pod™ Prime Nanometalene® Intervertebral Body Fusion Device.
Device ID | K162351 |
510k Number | K162351 |
Device Name: | SeaSpine® Vu A•POD™ Prime NanoMetalene® Intervertebral Body Fusion Device |
Classification | Intervertebral Fusion Device With Integrated Fixation, 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 | OVD |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-08-23 |
Decision Date | 2016-12-01 |
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 |