Ultrasonic Straight/Ultrasonic Knife/Ultrasonic Ring Currette
FDA 510(k) K020220 · Synergetics, Inc.
510(k) numberK020220
Submission
- Device name
- Ultrasonic Straight/Ultrasonic Knife/Ultrasonic Ring Currette
- Applicant
- Synergetics, Inc.
St. Charles, MO, US - Received
- January 22, 2002
- Decision date
- August 23, 2002
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- LFL – Instrument, Ultrasonic Surgical
- Device class
- Unclassified
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Questions and answers
When was Ultrasonic Straight/Ultrasonic Knife/Ultrasonic Ring Currette cleared by the FDA?
Ultrasonic Straight/Ultrasonic Knife/Ultrasonic Ring Currette (K020220) received a 510(k) decision of Substantially Equivalent on August 23, 2002, 213 days after the submission was received.
What is the product code of K020220?
The FDA product code is LFL – Instrument, Ultrasonic Surgical, a Unclassified device.