FDA 510(k) Applications Submitted by Sarah McIntyre
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K120016 |
01/03/2012 |
PIONEER STERNAL ASSIST IMPLANT SYSTEM |
PIONEER SURGICAL TECHNOLOGY, INC |
| K130427 |
02/20/2013 |
PIONEER ASPECT ANTERIOR CERVICAL PLATE SYSTEM |
PIONEER SURGICAL TECHNOLOGY, INC. |
| K120724 |
03/09/2012 |
PIONEER LATERAL PLATE SYSTEM |
PIONEER SURGICAL TECHNOLOGY, INC |
| K140696 |
03/19/2014 |
STREAMLINE TL SPINAL FIXATION SYSTEM |
PIONEER SURGICAL TECHNOLOGY, INC |
| K131100 |
04/19/2013 |
STREAMLINE TL SPINAL SYSTEM |
PIONEER SURGICAL TECHNOLOGY, INC |
| K111502 |
05/31/2011 |
STREAMLINE TL SPINAL SYSTEM |
PIONEER SURGICAL TECHNOLOGY, INC |
| K111528 |
06/02/2011 |
PIONEER ASPECT ANTERIOR CERVICAL PLATE MODEL 24-SERIES |
PIONEER SURGICAL TECHNOLOGY, INC |
| K121725 |
06/12/2012 |
PIONEER POSTERIOR OCCIPITO-CERVICO-THORACIC (OCT) SYSTEM |
PIONEER SURGICAL TECHNOLOGY, INC |
| K141600 |
06/16/2014 |
NANOSS BIOACTIVE, NANOSS BIOACTIVE LOADED, AND NANOSS BIOACTIVE LOADED KIT |
PIONEER SURGICAL TECHNOLOGY, INC. (RTI SURGICAL, I |
| K122293 |
07/31/2012 |
PIONEER STERNAL CABLE PLATE SYSTEM |
PIONEER SURGICAL TECHNOLOGY, INC |
| K142438 |
08/29/2014 |
Nerve Monitoring Cable System |
Pioneer Surgical Technology, Inc. (RTI Surgical, Inc.) |
| K133374 |
11/01/2013 |
STREAMLINE OCT OCCIPITO-CERVICO-THORACIC SYSTEM |
PIONEER SURGICAL TECHNOLOGY, INC. (RTI SURGICAL, I |
| K133623 |
11/26/2013 |
C-PLUS |
PIONEER SURGICAL TECHNOLOGY, INC |
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