Occlusion Clips

FDA 510(k) K760961 · Codman & Shurtleff, Inc.

Substantially Equivalent

510(k) numberK760961

Submission

Device name
Occlusion Clips
Applicant
Codman & Shurtleff, Inc.
Mchenry, IL, US
Received
October 29, 1976
Decision date
November 12, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HCH – Clip, Aneurysm
Device class
Class II (moderate risk)
Regulation
21 CFR 882.5200
Specialty
Neurology
Implant
Yes

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K211183Sugita AVM MicroclipsHCH · Traditional Mizuho America, Inc.03/02/2022SE
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K131500Yasargil Aneurysm Clips and Clip AppliersHCH · Traditional Aesculap, Inc.01/24/2014SE
K091921Codman Aneurysm Clips, Codman Avm Micro Clip System, Codman Slim-Line Graft…HCH · Special Codman & Shurtleff, Inc.09/08/2009SE
K081640Gimmi Aneurysm Clips and Applying ForcepsHCH · Abbreviated Gimmi GmbH05/06/2009SE
K081489L-Aneurysm-Clip System & L-Aneurysm Clip Appliers, Yasargil Aneurysm Clips & Yasargil…HCH · Traditional Peter Lazic GmbH09/25/2008SE
K060915Kirwan L-Aneurysm Clips and Applier, Kirwan Yasargil-Type Aneurysm Clips and AppliersHCH · Traditional Kirwan Surgical Products, Inc.04/17/2007SE
K043041Aesculap T-Bar Aneurysm Clips (Titanium & Phynox)HCH · Special Aesculap, Inc.12/09/2004SE
K032198Aesculap Yasargil Aneurysm Clip Phynox Booster ClipHCH · Special Aesculap, Inc.08/20/2003SE
K031468Temporary Titanium Aneurysm ClipHCH · Traditional Cardinalhealth06/20/2003SE

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Questions and answers

When was Occlusion Clips cleared by the FDA?

Occlusion Clips (K760961) received a 510(k) decision of Substantially Equivalent on November 12, 1976, 14 days after the submission was received.

What is the product code of K760961?

The FDA product code is HCH – Clip, Aneurysm, a Class II (moderate risk) device regulated under 21 CFR 882.5200.