Orbus Medical Technologies
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K041370 | LIFESTENT LP SDS BILIARY ENDOPROSTHESIS | FGE | 2004-06-24 | View |
| 510(k) | K041032 | MODIFICATION TO LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS | FGE | 2004-05-10 | View |
| 510(k) | K040550 | LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS | FGE | 2004-03-16 | View |
| 510(k) | K033212 | LIFESTENT SDS BILIARY ENDOPROSTHESIS | FGE | 2003-10-30 | View |
| 510(k) | K023308 | LIFESTENT SDS BILIARY ENDOPROSTHESIS, LIFESTENT XL SDS BILIARY ENDOPROSTHESIS | FGE | 2003-04-14 | View |
| 510(k) | K023121 | LIFESTENT BILIARY ENDOPROSTHESIS | FGE | 2003-03-10 | View |
| 510(k) | K023248 | LIFESTENT LP SDS BILIARY ENDOPROSTHESIS | FGE | 2003-02-11 | View |
| 510(k) | K010107 | R STENT BILIARY ENDOPROSTHESIS | FGE | 2001-07-31 | View |
No matching devices.
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