Smith & Nephew Inc., Endoscopy Division
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) | K121904 | GYNECOLOGY STERILIZATION TRAY | KCT | 2013-03-11 | View |
| 510(k) | K102982 | ENDOBUTTON DIRECT | MAI | 2011-01-05 | View |
| 510(k) | K082215 | OSTEORAPTOR SUTURE ANCHOR | JDR | 2008-11-03 | View |
| 510(k) | K081098 | ENDOBUTTON CONTINUOUS LOOP (CL) | JDR | 2008-07-16 | View |
| 510(k) | K072785 | TWINFIX FT PK | HWC | 2007-12-10 | View |
| 510(k) | K071586 | BIORAPTOR 2.3 PK SUTURE ANCHOR | MBI | 2007-08-17 | View |
| 510(k) | K070908 | SMITH & NEPHEW KINSA RC SUTURE ANCHOR | MBI | 2007-05-16 | View |
| 510(k) | K070167 | ENDOBUTTON DIRECT | MBI | 2007-04-12 | View |
No matching devices.
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