Entrigue Surgical, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K130354 | MEDIENT MIDDLE TURBINATE IMPLANT; (SINGLE PACK-1 PAIR, FOUR PACK-4 PAIR) | LYA | 2013-05-29 | View |
| 510(k) | K121351 | SINUS DILATION SYSTEM | LRC | 2012-08-29 | View |
| 510(k) | K082750 | ENTACT SEPTAL STAPLER, MODEL 610-00100 | OLL | 2009-01-06 | View |
| 510(k) | K072470 | BIOELAST 5-0 SUTURE, MODEL 500100 | NWJ | 2007-11-16 | View |
No matching devices.
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