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 |