Ace Stapler and Cartridge

FDA 510(k) K110829 · Barosense, Inc.

Substantially Equivalent

510(k) numberK110829

Submission

Device name
Ace Stapler and Cartridge
Applicant
Barosense, Inc.
Redwood City, CA, US
Received
March 24, 2011
Decision date
June 3, 2011
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
OCW – Endoscopic Tissue Approximation Device
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

To aid in endoscopically placing sutures, staples, clips, and other fastening tools through tissue.

Other 510(k)s with product code OCW

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K252400Endomina EZFuse systemOCW · Traditional Endo Tools Therapeutics S.A.02/13/2026SE
K243750SimpleStitch Suturing SystemOCW · Traditional Envision Endoscopy04/17/2025SE
K231240MaxTack™ Motorized Fixation DeviceOCW · Traditional Covidien09/08/2023SE
K213271MedicloseTM SystemOCW · Traditional Health Value Creation B.V., Trading AS Corporis…08/31/2023SE
K231553OverStitch NXT Endoscopic Suturing SystemOCW · Special Apollo Endosurgery, Inc.06/29/2023SE
K211309endomina systemOCW · Traditional Endo Tools Therapeutics S.A.12/07/2021SE
K201744Su2ura Approximation DeviceOCW · Traditional Anchora Medical, Ltd.06/17/2021SE
K210266OverStitch Sx Endoscopic Suturing SystemOCW · Special Apollo Endosurgery, Inc.03/02/2021SE
K193652AbClose - Port Site Closure DeviceOCW · Traditional Medeon Biodesign, Inc.03/26/2020SE
K191439OverStitch 2-0 Polypropylene SutureOCW · Traditional Apollo Endosurgery08/29/2019SE

More from Apollo Endosurgery

510(k)DeviceDecision
K120126Barosense Endogastric Tube and Introducer BougieFED · Special 09/10/2012SE
K120147Ace Stapler and CartridgeOCW · Special 02/17/2012SE
K082044Ace Stapler, Model F0031OCW · Traditional 05/11/2010SE
K082589Barosense Endogastric Tube (Egt), Model F0034FED · Traditional 05/22/2009SE

Questions and answers

When was Ace Stapler and Cartridge cleared by the FDA?

Ace Stapler and Cartridge (K110829) received a 510(k) decision of Substantially Equivalent on June 3, 2011, 71 days after the submission was received.

What is the product code of K110829?

The FDA product code is OCW – Endoscopic Tissue Approximation Device, a Class II (moderate risk) device regulated under 21 CFR 876.1500.