The following data is part of a premarket notification filed by Pioneer Surgical Technology, Inc., Dba Rti Surgical, Inc. with the FDA for Fortilink Interbody Fusion Device (ibf) With Tetrafuse 3d Technology.
| Device ID | K192718 |
| 510k Number | K192718 |
| Device Name: | Fortilink Interbody Fusion Device (IBF) With TETRAfuse 3D Technology |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | Pioneer Surgical Technology, Inc., DBA RTI Surgical, Inc. 375 River Park Circle Marquette, MI 49855 -0627 |
| Contact | Linda Busklein |
| Correspondent | Linda Busklein Pioneer Surgical Technology, Inc., DBA RTI Surgical, Inc. 375 River Park Circle Marquette, MI 49855 -0627 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-09-27 |
| Decision Date | 2019-12-20 |