K020220 is an FDA 510(k) clearance for the ULTRASONIC STRAIGHT/ULTRASONIC KNIFE/ULTRASONIC RING CURRETTE, a Instrument, Ultrasonic Surgical, submitted by Synergetics, Inc. (St. Charles, US). The FDA issued a Cleared decision on August 23, 2002, 213 days after receiving the submission on January 22, 2002. This device falls under the General & Plastic Surgery review panel.
| 510(k) Number | K020220 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | January 22, 2002 |
| Decision Date | August 23, 2002 |
| Days to Decision | 213 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | LFL — Instrument, Ultrasonic Surgical |
| Device Class | — |