Reprocessed Used Disposable Arthroscopic Blades and Burs

FDA 510(k) K022744 · Medical Device Services

Substantially Equivalent

510(k) numberK022744

Submission

Device name
Reprocessed Used Disposable Arthroscopic Blades and Burs
Applicant
Medical Device Services
St. George, UT, US
Received
August 19, 2002
Decision date
September 18, 2002
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HWE – Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
Device class
Class I (low risk)
Regulation
21 CFR 878.4820
Specialty
General, Plastic Surgery

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K063688Surgical Irrigation System, Irrigation TubeHWE · Special The Anspach Effort, Inc.01/16/2007SE
K050766Explant Osteonecrosis Intervention Implant Removal SystemHWE · Traditional Zimmer Trabecular05/26/2005SE
K043310Synthes (USA) Electric Pen Drive SystemHWE · Traditional Synthes (Usa)01/05/2005SE
K012694Reprocessed Used Disposable Arthroscopic Blades and BursHWE · Traditional Adven Medical02/04/2002SE
K012676Reprocessed Used, Disposable Blades, Burs, Bits and TapsHWE · Traditional Adven Medical02/04/2002SE
K990816Avcore SystemHWE · Traditional Modular Cutting Systems, Inc.09/24/1999SE
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K973560Bone Graft HarvesterHWE · Traditional Ds Mfg., Inc.11/12/1997SE

More from Ds Mfg., Inc.

510(k)DeviceDecision
K022753Reprocesses Used Disposable Sequential Compression Sleeves/WrapsJOW · Traditional 11/14/2002SE
K022751Reprocessed Used Disposable Hot and Cold Biopsy ForcepsKGE · Traditional 11/04/2002SE
K022748Reprocssed Used Disposable Endoscopic Scissors and GraspersHET · Traditional 10/09/2002SE
K022743Reprocessed Disposable TrocarsKAB · Traditional 10/09/2002SE
K012979Compressible Limb SleeveJOW · Traditional 05/08/2002SE

Questions and answers

When was Reprocessed Used Disposable Arthroscopic Blades and Burs cleared by the FDA?

Reprocessed Used Disposable Arthroscopic Blades and Burs (K022744) received a 510(k) decision of Substantially Equivalent on September 18, 2002, 30 days after the submission was received.

What is the product code of K022744?

The FDA product code is HWE – Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment, a Class I (low risk) device regulated under 21 CFR 878.4820.