Bonutti Research, Inc.
Bonutti Research, Inc. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2016.
Top product codes for Bonutti Research, Inc.
Recent clearances by Bonutti Research, Inc.
- K161628 — JAS Pulse(TM) Ultrasonic Therapy
- K093078 — UNITY ULTRASONIC SYSTEM WITH PLLA ANCHORS
- K090175 — UNITY BETA PLLA SYSTEM
- K082906 — UNITY BETA ANCHOR SYSTEM
- K062820 — UNITY ALPHA SYSTEM
- K060283 — TRANSET SYSTEM
- K052799 — MULTITAK 6.0 MM ABSORBABLE ANCHOR SYSTEM
- K033717 — TRANSET FRACTURE FIXATION SYSTEM
- K013177 — MULTITAK SUTURE SNAP SYSTEM
- K012465 — MULTITAK SPLINTER 3.0 MM RESORBABLE ANCHOR
- K010479 — MULTITAK CONICAL TIP BONE SOFT TISSUE SUTURE ANCHOR
- K993115 — MULTITAK SS
Data sourced from openFDA. This site is unofficial and independent of the FDA.