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Pioneer Surgical Technology

7 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Pioneer Quantum Spinal Rod System, MIS Yoke Manipulator, Long Slot, non-sterile; Cat # 51- recall (Z-0291-2008)Pioneer Surgical Technology2007-11-27
Zimmer Cannulated Screw System Cannulated Driver, 5.0 mm Hex, REF 1147-49-50; Catalog # 00 recall (Z-0872-06)Pioneer Surgical Technology2006-05-18
Pioneer Surgical brand Quantum Spinal Rod System Polyaxial Screw, length 45 mm; Catalog nu recall (Z-0020-06)Pioneer Surgical Technology2005-10-07
Pioneer Surgical brand Quantum Spinal Rod System Polyaxial Screw, length 40 mm; Catalog nu recall (Z-0021-06)Pioneer Surgical Technology2005-10-07
Pioneer Surgical brand Quantum Spinal Rod System Locking Cap; Catalog No 10-LCAP. recall (Z-1457-05)Pioneer Surgical Technology2005-08-31
Stayfuse brand intramedullary bone screw; MID 3.8 x 6 mm. Zimmer part number 00-2227-003-0 recall (Z-0561-04)Pioneer Surgical Technology2004-02-27
StayFuse PROX 03.3 MM sterile intramedullary bone screw distributed by Zimmer recall (Z-0948-03)Pioneer Surgical Technology2003-06-21

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Every clearance here is in the API, with alerts when new ones post.