The following data is part of a premarket notification filed by Rti Surgical, Inc. with the FDA for Fortilink® Interbody Fusion (ibf) System With Tetrafuse® 3d Technology.
| Device ID | K172343 |
| 510k Number | K172343 |
| Device Name: | Fortilink® Interbody Fusion (IBF) System With TETRAfuse® 3D Technology |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | RTI Surgical, Inc. 11621 Research Circle Alachua, FL 32615 |
| Contact | Diana Taylor |
| Correspondent | Diana Taylor RTI Surgical, Inc. 375 River Park Circle Marquette, MI 49855 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-08-02 |
| Decision Date | 2017-10-23 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FORTILINK 87101032 5287571 Live/Registered |
Pioneer Surgical Technology, Inc. 2016-07-12 |