The following data is part of a premarket notification filed by Innovasive, Inc. with the FDA for Dualx.
Device ID | K181397 |
510k Number | K181397 |
Device Name: | DualX |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | Innovasive, Inc. 26020 Acero, Ste 200 Mission Viejo, CA 92691 |
Contact | Andy Choi |
Correspondent | Meredith L. May Empirical Consulting 4628 Northpark Drive Colorado Springs, CO 80918 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-05-29 |
Decision Date | 2018-09-27 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DUALX 87198136 5788186 Live/Registered |
IMDS, LLC 2016-10-10 |