FORTICORE
Intervertebral Fusion Device With Bone Graft, Cervical
NANOVIS, LLC
The following data is part of a premarket notification filed by Nanovis, Llc with the FDA for Forticore.
Pre-market Notification Details
| Device ID | K140280 |
| 510k Number | K140280 |
| Device Name: | FORTICORE |
| Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
| Applicant | NANOVIS, LLC PO BOX 566 Chesterland, OH 44026 |
| Contact | Karen E Warden Phd |
| Correspondent | Karen E Warden Phd NANOVIS, LLC PO BOX 566 Chesterland, OH 44026 |
| Product Code | ODP |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-02-04 |
| Decision Date | 2014-09-05 |
| Summary: | summary |
Trademark Results [FORTICORE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 FORTICORE 88191764 not registered Live/Pending |
Incipio, LLC 2018-11-13 |
 FORTICORE 86428545 5008687 Live/Registered |
FORTINET, INC. 2014-10-20 |
 FORTICORE 85740388 4660083 Live/Registered |
Nanovis, LLC 2012-09-27 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.