The following data is part of a premarket notification filed by Pioneer Surgical Technology, Inc with the FDA for Streamline Tl Spinal Fixation System.
Device ID | K140696 |
510k Number | K140696 |
Device Name: | STREAMLINE TL SPINAL FIXATION SYSTEM |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | PIONEER SURGICAL TECHNOLOGY, INC 375 RIVER PARK CIRCLE Marquette, MI 49855 |
Contact | Sarah Mcintyre |
Correspondent | Sarah Mcintyre PIONEER SURGICAL TECHNOLOGY, INC 375 RIVER PARK CIRCLE Marquette, MI 49855 |
Product Code | NKB |
Subsequent Product Code | KWQ |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-03-19 |
Decision Date | 2014-04-10 |
Summary: | summary |