# K960374: Ultracut 2000

- Pathway: 510(k) (Traditional)
- Applicant: Ultralase Technologies, Inc.
- Decided: Jun 28, 1996 after 154 days
- Product code: LFL (Instrument, Ultrasonic Surgical)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K801623 (1980). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K801623: Cavitron Ultrasonic Surg. Aspir. Cusa, Cavitron Corp. (1980) Summary page 1.

## Indications for use
The Ultracut 2000 and CUSA are both ultrasonic surgical instruments intended for use to cut or fragment tissue, bone, or organs in orthopedic surgery.

Source page: https://510kreport.com/device/K960374
Methodology: https://510kreport.com/methodology