The following data is part of a premarket notification filed by Pioneer Surgical Technology, Inc. with the FDA for Streamline Mis Spinal Fixation System.
Device ID | K192396 |
510k Number | K192396 |
Device Name: | Streamline MIS Spinal Fixation System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Pioneer Surgical Technology, Inc. (DBA RTI Surgical Inc.) 375 River Park Circle Marquette, MI 49855 |
Contact | Michael Mach |
Correspondent | Michael Mach Pioneer Surgical Technology, Inc. (DBA RTI Surgical Inc.) 375 River Park Circle Marquette, MI 49855 |
Product Code | NKB |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-09-03 |
Decision Date | 2019-11-26 |
Summary: | summary |