The following data is part of a premarket notification filed by Pioneer Surgical Technology, Inc. (dba Rti Surgical, Inc.) with the FDA for Streamline Oct Occipito-cervico-thoracic System.
Device ID | K150254 |
510k Number | K150254 |
Device Name: | Streamline OCT Occipito-Cervico-Thoracic System |
Classification | Appliance, Fixation, Spinal Interlaminal |
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 | KWP |
CFR Regulation Number | 888.3050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-02-03 |
Decision Date | 2015-04-28 |
Summary: | summary |