FDA 510(k) Applications Submitted by EMILY M DOWNS
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K132050 |
07/02/2013 |
NB3D BONE VOID FILLER |
PIONEER SURGICAL TECHNOLOGY, INC |
| K133455 |
11/12/2013 |
CROSSFUSE II CORONAL TAPER, CROSSFUSE II HYPERLORDOTIC |
PIONEER SURGICAL TECHNOLOGY, INC |
| K093771 |
12/08/2009 |
QUANTUM/STREAMLINE TL MIS SPINAL SYSTEM |
PIONEER SURGICAL TECHNOLOGY |
| K133785 |
12/12/2013 |
TRITIUM STERNAL CABLE PLATE SYSTEM |
PIONEER SURGICAL TECHNOLOGY, INC |
| K130286 |
02/05/2013 |
STREAMLINE MIS SPINAL FIXATION SYSTEM |
PIONEER SURGICAL TECHNOLOGY, INC |
| K110367 |
02/08/2011 |
PIONEER SPINAL PROCESS FUSION PLATE |
PIONEER SURGICAL TECHNOLOGY, INC |
| K110692 |
03/11/2011 |
STREAMLINE TL SPINAL SYSTEM |
PIONEER SURGICAL TECHNOLOGY, INC. |
| K100708 |
03/12/2010 |
PIONEER ANTERIOR CERVICAL PLATE MODEL 24-SERIES |
PIONEER SURGICAL TECHNOLOGY |
| K131724 |
06/12/2013 |
PIONEER MAXFUSE VERTEBRAL BODY REPLACEMENT DEVICE |
PIONEER SURGICAL TECHNOLOGY, INC |
| K092295 |
07/29/2009 |
PIONEER POSTERIOR CERVICO-THORACIC SYSTEM |
PIONEER SURGICAL TECHNOLOGY |
| K112496 |
08/29/2011 |
PIONEER CROSSFUSE II IBF/VBR SYSTEM |
PIONEER SURGICAL TECHNOLOGY, INC. |
| K112757 |
09/22/2011 |
PIONEER POSTERIOR CERVICO THORACIC SYSTEM |
PIONEER SURGICAL TECHNOLOGY, INC. |
| K102903 |
09/30/2010 |
PIONEER CANNULATED SCREW SYSTEM |
PIONEER SURGICAL TECHNOLOGY, INC. |
| K093692 |
11/30/2009 |
QUANTUM/ STREAMLINE SPINAL SYSTEM MODEL 02-SERIES AND 10-SERIES |
PIONEER SURGICAL TECHNOLOGY |
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