The following data is part of a premarket notification filed by Pioneer Surgical Technology, Inc. (dba Rti Surgical, Inc.) with the FDA for Cervalign™ Anterior Cervical Plate System.
Device ID | K183060 |
510k Number | K183060 |
Device Name: | CervAlign™ Anterior Cervical Plate System |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.) 375 River Park Circle Marquette, MI 49855 |
Contact | Jaclyn Holli |
Correspondent | Jaclyn Holli Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.) 375 River Park Circle Marquette, MI 49855 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-11-02 |
Decision Date | 2019-01-17 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CERVALIGN 88037029 not registered Live/Pending |
Pioneer Surgical Technology, Inc. 2018-07-13 |