# K010666: XPS 3000 System with Reciprocating Adapter and Suction Cannulae

- Pathway: 510(k) (Traditional)
- Applicant: Medtronic Xomed, Inc.
- Decided: May 7, 2001 after 62 days
- Product code: QPB (System, Suction, Lipoplasty For Removal)
- Device class: 2
- Regulation: 21 CFR 878.5040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K832520 (1983). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K992855: XPS Straightshot or Model 2000 Microdebrider System or XPS Powersculpt, Xomed, Inc. (2000) Summary page 6.

## Indications for use
The XPS 3000 system with reciprocating adapter and suction cannlua is intended for the removal of soft tissue and fluid during general surgical procedures including suction lipoplasty for aesthetic body contouring.

Source page: https://510kreport.com/device/K010666
Methodology: https://510kreport.com/methodology