Pioneer Surgical Technology - FDA 510(k) Cleared Devices
50
Total
48
Cleared
0
Denied
Pioneer Surgical Technology has 48 FDA 510(k) cleared orthopedic devices. Based in Marquette, US.
Historical record: 48 cleared submissions from 1993 to 2011.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
50 devices
Cleared
Apr 29, 2011
FORTROSS BONE VOID FILLER
Orthopedic
60d
Cleared
Mar 07, 2011
QUANTUM SPINAL SYSTEM, QUANTUM MIS
Orthopedic
252d
Cleared
Oct 22, 2010
PIONEER SPINOUS PROCESS FUSION PLATE
Orthopedic
142d
Cleared
Aug 11, 2010
QUANTUM/ STREAMLINE SPINAL SYSTEM MODEL 02-SERIES AND 10-SERIES
Orthopedic
254d
Cleared
Aug 10, 2010
QUANTUM/STREAMLINE TL MIS SPINAL SYSTEM
Orthopedic
245d
Cleared
Jun 04, 2010
PIONEER ANTERIOR CERVICAL PLATE MODEL 24-SERIES
Orthopedic
84d
Cleared
Apr 22, 2010
NANOSS BONE VOID FILLER
Orthopedic
69d
Cleared
Feb 19, 2010
PIONEER POSTERIOR CERVICO-THORACIC SYSTEM
Orthopedic
205d
Cleared
Nov 17, 2009
PIONEER SURGICAL NANOSS BVF-E
Orthopedic
221d
Cleared
Jun 12, 2009
E-MATRIX GRAFT BONE EXTENDER
Orthopedic
203d
Cleared
Apr 28, 2009
PIONEER LUMBAR PLATE SYSTEM
Orthopedic
88d
Cleared
Feb 25, 2009
PACP
Orthopedic
77d
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