The following data is part of a premarket notification filed by Rti Surgical, Inc. Dba Rti Biologics with the FDA for Interbody Fusion (ibf)/vertebral Body Replacement (vbr) System.
Device ID | K170643 |
510k Number | K170643 |
Device Name: | Interbody Fusion (IBF)/Vertebral Body Replacement (VBR) System |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | RTI Surgical, Inc. Dba RTI Biologics 11621 Research Circle Alachua, FL 32615 |
Contact | Jennifer Bonacci |
Correspondent | Jennifer Bonacci RTI Surgical, Inc. Dba RTI Biologics 11621 Research Circle Alachua, FL 32615 |
Product Code | MAX |
Subsequent Product Code | MQP |
Subsequent Product Code | ODP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-03-02 |
Decision Date | 2017-04-14 |
Summary: | summary |