Xylos Corporation
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K111584 | XYLOS MACRO-POROUS SURGICAL MESH | FTM | 2011-08-25 | View |
| 510(k) | K100984 | XYLOS VESSEL GUARD | OMR | 2010-07-07 | View |
| 510(k) | K090880 | XYLOS POROUS SURGICAL MESH | FTM | 2009-05-27 | View |
| 510(k) | K090778 | MTA PROTECTIVE SHEET | FTM | 2009-04-28 | View |
| 510(k) | K083823 | SECURIAN TISSUE REINFORCEMENT MATRIX | FTM | 2009-03-18 | View |
| 510(k) | K081882 | MODIFICATION TO XYLOS SURGICAL MESH | FTM | 2008-07-11 | View |
| 510(k) | K023237 | XYLOS SURGICAL MESH | FTM | 2003-03-18 | View |
| 510(k) | K024054 | XYLOS XCELL ANTIMICROBIAL DRESSING | MGQ | 2003-03-07 | View |
| 510(k) | K974251 | X-CELL WOUND DRESSING | MGQ | 1998-06-22 | View |
No matching devices.
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