Coaxial Accordion Stone Management Device, Model: COAC12005 - COA20015

FDA 510(k) K082803 · Percutaneous Systems, Inc.

Substantially Equivalent

510(k) numberK082803

Submission

Device name
Coaxial Accordion Stone Management Device, Model: COAC12005 - COA20015
Applicant
Percutaneous Systems, Inc.
Palo Alto, CA, US
Received
September 24, 2008
Decision date
November 13, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FFL – Dislodger, Stone, Basket, Ureteral, Metal
Device class
Class II (moderate risk)
Regulation
21 CFR 876.4680
Specialty
Gastroenterology, Urology

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More from Olympus America, Inc.

510(k)DeviceDecision
K102887Accordion Stone Management Device Model AC281205 and AC3814510FFL · Traditional 05/16/2011SE
K090485Coaxial Accordion Ercp Device, Models C0AC19001, COAC20005, COAC22003LQR · Traditional 07/22/2009SE
K061766Expressway Intermittent CatheterEZD · Traditional 03/09/2007SE
K052298Cystoglide Introducer SheathKNY · Traditional 12/12/2006SE
K052134Cystoglide Dilating Introducer SheathKNY · Traditional 09/22/2005SE
K052048AccordionFFL · Traditional 09/13/2005SE
K042531Updated Slip Urology Introducer SheathKNY · Special 02/01/2005SE
K042877Microverter Ureteral Access SheathKNY · Traditional 11/16/2004SE
K040520Slip Urology Introducer SheathKNY · Traditional 05/20/2004SE
K040519Slip Urology CatheterEZD · Traditional 05/20/2004SE

Questions and answers

When was Coaxial Accordion Stone Management Device, Model: COAC12005 - COA20015 cleared by the FDA?

Coaxial Accordion Stone Management Device, Model: COAC12005 - COA20015 (K082803) received a 510(k) decision of Substantially Equivalent on November 13, 2008, 50 days after the submission was received.

What is the product code of K082803?

The FDA product code is FFL – Dislodger, Stone, Basket, Ureteral, Metal, a Class II (moderate risk) device regulated under 21 CFR 876.4680.