Disc-O-Tech Medical Technologies, Ltd.
FDA 510(k) & PMA Approved Devices — 16 products
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Total Devices16
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K071375 | MESH FENESTRATED INTRODUCER NEEDLE (MESH INTRODUCER NEEDLE) | NDN | 2007-12-21 | View |
| 510(k) | K071679 | METAFIX AND FIXION FA INTRAMEDULLARY NAILING SYSTEMS | HSB | 2007-12-17 | View |
| 510(k) | K063067 | CONFIDENCE FENESTRATED INTRODUCER NEEDLE | NDN | 2006-11-03 | View |
| 510(k) | K062424 | CONFIDENCE EX HIGH VISCOSITY BONE CEMENT | NDN | 2006-09-14 | View |
| 510(k) | K060300 | CONFIDENCE HIGH VISCOSITY BONE CEMENT | NDN | 2006-06-21 | View |
| 510(k) | K040612 | SKY BONE EXPANDER SYSTEM (SKY SYSTEM) | HRX | 2004-06-17 | View |
| 510(k) | K040939 | SKY BONE EXPANDER SYSTEM (SKY SYSTEM) | HRX | 2004-05-12 | View |
| 510(k) | K032730 | FIXION HIP SYSTEM | JDI | 2004-03-26 | View |
| 510(k) | K034037 | SKY BONE EXPANDER SYSTEM | HRX | 2004-01-28 | View |
| 510(k) | K032358 | B-TWIN BONE EXPANDER SYSTEM (B-TWIN BE SYSTEM) | HRX | 2003-12-17 | View |
| 510(k) | K030972 | FIXION UNIPOLAR MODULAR HEMI-HIP SYSTEM (FIXION MH) | KWL | 2003-05-30 | View |
| 510(k) | K014072 | FIXION UNIPOLAR MODULAR HEMI-HIP SYSTEM (FIXION UH) | KWY | 2002-03-08 | View |
| 510(k) | K013449 | MODIFICATION TO FIXION INTERLOCKING INTRAMEDULLARY NAILING SYSTEM | HSB | 2001-12-19 | View |
| 510(k) | K010988 | FIXION INTERLOCKING PROXIMAL FEMORAL NAILING SYSTEM | HSB | 2001-06-19 | View |
| 510(k) | K010901 | FIXION INTRAMEDULLARY NAILING SYSTEM (FIXION IMN) MODEL B | HSB | 2001-06-19 | View |
| 510(k) | K011390 | BONUS-ORTHOPEDIC BONE SCREW FIXATION SYSTEM | MBI | 2001-06-06 | View |
No matching devices.
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