# K992855: XPS Straightshot or Model 2000 Microdebrider System or XPS Powersculpt

- Pathway: 510(k) (Traditional)
- Applicant: Xomed, Inc.
- Decided: Jan 21, 2000 after 150 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: 1 generation back to K832520 (1983). 2 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K981922: Light Duty Pneumatic Instrument Model Number Pad-100, Heavy Duty Pneumatic Instrument Model Pad-200, Light Duty Electri, Microaire Surgical Instruments, Inc. (1998) Summary page 6.
- K832520: Suction Tips, Wells Johnson Co. (1983) Summary page 6.
- (no number) NuMED Power Cannula: named in the summary without a submission number

## Most influential descendants
- K021813: Hydrocision General Surgery Fluidjet System (2003), 0 descendants of its own
- K010666: XPS 3000 System with Reciprocating Adapter and Suction Cannulae (2001), 0 descendants of its own

## Indications for use
The XPS/PowerSculpt System with reciprocating adapter and suction cannula is indicated for the removal of soft tissue and fluid from the body during general surgical procedures including suction lipoplasty for aesthetic body contouring.

Source page: https://510kreport.com/device/K992855
Methodology: https://510kreport.com/methodology