Bonutti Research, Inc.
FDA 510(k) & PMA Approved Devices — 12 products
Advertisement
Total Devices12
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K161628 | JAS Pulse(TM) Ultrasonic Therapy | IMI | 2016-11-10 | View |
| 510(k) | K093078 | UNITY ULTRASONIC SYSTEM WITH PLLA ANCHORS | HWC | 2010-06-23 | View |
| 510(k) | K090175 | UNITY BETA PLLA SYSTEM | HWC | 2009-09-10 | View |
| 510(k) | K082906 | UNITY BETA ANCHOR SYSTEM | HWC | 2008-10-30 | View |
| 510(k) | K062820 | UNITY ALPHA SYSTEM | HWC | 2007-03-15 | View |
| 510(k) | K060283 | TRANSET SYSTEM | HTY | 2006-02-22 | View |
| 510(k) | K052799 | MULTITAK 6.0 MM ABSORBABLE ANCHOR SYSTEM | MAI | 2005-12-16 | View |
| 510(k) | K033717 | TRANSET FRACTURE FIXATION SYSTEM | HTY | 2004-02-25 | View |
| 510(k) | K013177 | MULTITAK SUTURE SNAP SYSTEM | GAM | 2001-12-19 | View |
| 510(k) | K012465 | MULTITAK SPLINTER 3.0 MM RESORBABLE ANCHOR | MAI | 2001-10-29 | View |
| 510(k) | K010479 | MULTITAK CONICAL TIP BONE SOFT TISSUE SUTURE ANCHOR | HTY | 2001-05-08 | View |
| 510(k) | K993115 | MULTITAK SS | MAI | 1999-12-17 | View |
No matching devices.
Advertisement