XPS Tissue Aspiration System, XPS Straightshot or Model 2000 Microdebrider System

FDA 510(k) K984363 · Xomed, Inc.

Substantially Equivalent

510(k) numberK984363

Submission

Device name
XPS Tissue Aspiration System, XPS Straightshot or Model 2000 Microdebrider System
Applicant
Xomed, Inc.
Jacksonville, FL, US
Received
December 7, 1998
Decision date
February 26, 1999
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
BTA – Pump, Portable, Aspiration (Manual Or Powered)
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

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More from Shenzhen Kingboom Technology Co., Ltd.

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
K992855XPS Straightshot or Model 2000 Microdebrider System or XPS PowersculptQPB · Traditional 01/21/2000SE
K993582Modification to Laser-Shield IIBTR · Traditional 01/20/2000SE
K993655Micro-France Electrosurgical Instruments, VariousGEI · Traditional 12/21/1999SE

Questions and answers

When was XPS Tissue Aspiration System, XPS Straightshot or Model 2000 Microdebrider System cleared by the FDA?

XPS Tissue Aspiration System, XPS Straightshot or Model 2000 Microdebrider System (K984363) received a 510(k) decision of Substantially Equivalent on February 26, 1999, 81 days after the submission was received.

What is the product code of K984363?

The FDA product code is BTA – Pump, Portable, Aspiration (Manual Or Powered), a Class II (moderate risk) device regulated under 21 CFR 878.4780.