XPS Straightshot or Model 2000 Microdebrider System or XPS Powersculpt

FDA 510(k) K992855 · Xomed, Inc.

Substantially Equivalent

510(k) numberK992855

Submission

Device name
XPS Straightshot or Model 2000 Microdebrider System or XPS Powersculpt
Applicant
Xomed, Inc.
Jacksonville, FL, US
Received
August 24, 1999
Decision date
January 21, 2000
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
QPB – System, Suction, Lipoplasty For Removal
Device class
Class II (moderate risk)
Regulation
21 CFR 878.5040
Specialty
General, Plastic Surgery

A suction lipoplasty system is a device intended for the removal of adipose tissue for purposes of aesthetic body contouring

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K244026PAL 7020 ConsoleQPB · Traditional Microaire Surgical Instruments, LLC04/25/2025SE
K242804PAL Aspiration SystemQPB · Traditional Microaire Surgical Instruments, LLC12/30/2024SE
K241835AirSculpt Body Contouring System (AIRS-1-SYS)QPB · Traditional Cellmyx11/27/2024SE
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More from Black & Black Surgical, Inc.

510(k)DeviceDecision
K002395Model 30 Classic PneumatonometerHKX · Traditional 12/11/2000SE
K002987Redtronic Xomed Monopolar Energized BladeGEI · Traditional 12/04/2000SE
K002828XPS Nitro SystemERL · Traditional 10/17/2000SE
K002897Titanium Middle Ear ProsthesesETB · Traditional 10/11/2000SE
K993653Micro-France Trocars and AccessoriesHET · Traditional 06/09/2000SE
K001148Merogel Otologic PackKHJ · Traditional 06/03/2000SE
K994262Frontal Sinus Trephination CannulaKAM · Traditional 02/08/2000SE
K993582Modification to Laser-Shield IIBTR · Traditional 01/20/2000SE
K993655Micro-France Electrosurgical Instruments, VariousGEI · Traditional 12/21/1999SE
K993112Xomed ENT RF SystemGEI · Traditional 12/09/1999SE

Questions and answers

When was XPS Straightshot or Model 2000 Microdebrider System or XPS Powersculpt cleared by the FDA?

XPS Straightshot or Model 2000 Microdebrider System or XPS Powersculpt (K992855) received a 510(k) decision of Substantially Equivalent on January 21, 2000, 150 days after the submission was received.

What is the product code of K992855?

The FDA product code is QPB – System, Suction, Lipoplasty For Removal, a Class II (moderate risk) device regulated under 21 CFR 878.5040.