The following data is part of a premarket notification filed by Pioneer Surgical Technology, Inc. Dba Rti Surgical, Inc. with the FDA for Unison-c Anterior Cervical Fixation System.
Device ID | K170830 |
510k Number | K170830 |
Device Name: | Unison-C Anterior Cervical Fixation System |
Classification | Intervertebral Fusion Device With Integrated Fixation, Cervical |
Applicant | Pioneer Surgical Technology, Inc. DBA RTI Surgical, Inc. 375 River Park Circle Marquette, MI 49855 |
Contact | Sarah Pleaugh |
Correspondent | Sarah Pleaugh Pioneer Surgical Technology, Inc. DBA RTI Surgical, Inc. 375 River Park Circle Marquette, MI 49855 |
Product Code | OVE |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-03-20 |
Decision Date | 2017-06-28 |
Summary: | summary |