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 |