Pioneer Surgical Technology
FDA 510(k) & PMA Approved Devices — 50 products
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Total Devices50
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K110561 | FORTROSS BONE VOID FILLER | MQV | 2011-04-29 | View |
| 510(k) | K101790 | QUANTUM SPINAL SYSTEM, QUANTUM MIS | NKB | 2011-03-07 | View |
| 510(k) | K101525 | PIONEER SPINOUS PROCESS FUSION PLATE | KWP | 2010-10-22 | View |
| 510(k) | K093692 | QUANTUM/ STREAMLINE SPINAL SYSTEM MODEL 02-SERIES AND 10-SERIES | NKB | 2010-08-11 | View |
| 510(k) | K093771 | QUANTUM/STREAMLINE TL MIS SPINAL SYSTEM | MNH | 2010-08-10 | View |
| 510(k) | K100708 | PIONEER ANTERIOR CERVICAL PLATE MODEL 24-SERIES | KWQ | 2010-06-04 | View |
| 510(k) | K100361 | NANOSS BONE VOID FILLER | MQV | 2010-04-22 | View |
| 510(k) | K092295 | PIONEER POSTERIOR CERVICO-THORACIC SYSTEM | KWP | 2010-02-19 | View |
| 510(k) | K091031 | PIONEER SURGICAL NANOSS BVF-E | MQV | 2009-11-17 | View |
| 510(k) | K083449 | E-MATRIX GRAFT BONE EXTENDER | MQV | 2009-06-12 | View |
| 510(k) | K090222 | PIONEER LUMBAR PLATE SYSTEM | KWQ | 2009-04-28 | View |
| 510(k) | K083663 | PACP | KWQ | 2009-02-25 | View |
| 510(k) | K081558 | PIONEER SURGICAL TECHNOLOGY NANOSS BVF-E, MODELS 5, 10, 20CC | MQV | 2008-08-25 | View |
| 510(k) | K073229 | NERVE MONITORING CABLE | GXZ | 2008-06-06 | View |
| 510(k) | K073177 | PIONEER INTERVERTEBRAL FUSION DEVICE SYSTEM | MAX | 2008-05-13 | View |
| 510(k) | K080504 | PIONEER LOWTOP SPINAL ROD SYSTEM | NKB | 2008-03-20 | View |
| 510(k) | K080518 | PIONEER SURGICAL TECHNOLOGY QUANTUM SPINAL SYSTEM | NKB | 2008-03-20 | View |
| 510(k) | K080026 | QUANTUM-MIS CANNULATED SYSTEM | MNI | 2008-01-28 | View |
| 510(k) | K072703 | PIONEER SLIMFUSE ANTERIOR CERVICAL PLATING SYSTEM | KWQ | 2008-01-10 | View |
| 510(k) | K072187 | PIONEER LOWTOP SPINAL ROD SYSTEM | MNI | 2007-10-12 | View |
No matching devices.
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