Codman * Reusable Perforator

FDA 510(k) K820087 · Codman & Shurtleff, Inc.

Substantially Equivalent

510(k) numberK820087

Submission

Device name
Codman * Reusable Perforator
Applicant
Codman & Shurtleff, Inc.
Mchenry, IL, US
Received
January 13, 1982
Decision date
February 4, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HBF – Drills, Burrs, Trephines & Accessories (Compound, Powered)
Device class
Class II (moderate risk)
Regulation
21 CFR 882.4305
Specialty
Neurology

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K254177Disposable Sterile Skull Drill (LZ)HBF · Traditional Guizhou Zirui Technology Co., Ltd.09/11/2026SE
K231403evoDrill Cranial PerforatorHBF · Traditional Evonos GmbH & Co. KG03/06/2024SE
K213228NeuroLine Disposable Cranial Perforator with Hudson endHBF · Traditional Emd Endoszkop Muszer Gyarto ES Kereskedelmi Kft.06/20/2022SE
K183581Codman Disposable PerforatorsHBF · Special Integra Lifesciences Corp.01/20/2019SE
K141455Easydrill Autostop Cranial PerforatorHBF · Traditional Micromar Ind. Com. , Ltd.03/16/2015SE
K121253Meridian Cranial PerforatorHBF · Traditional Adeor Medical Technologies GmbH07/17/2012SE
K082010Stryker Disposable Cranial Perforator BitHBF · Traditional Stryker Ireland Ltd., Instruments Division12/29/2008SE
K082637Cranial PerforatorHBF · Traditional The Anspach Effort, Inc.12/22/2008SE
K073336Codman Craniotomy Kit, Models 26-1229, 26-1230, 26-1231HBF · Special Codman & Shurtleff, Inc.01/04/2008SE
K071931Codman Disposable Perforator, Model(S) 26-1222, 26-1223HBF · Traditional Codman & Shurtleff, Inc.10/22/2007SE

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K172022CODMAN Hydrocephalus Valves, Catheters & Accessories (Bundled)JXG · Traditional 10/03/2017SE
K171862GALAXY G3 Mini Microcoil Delivery SystemHCG · Traditional 09/25/2017SE
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K171653YOGA Microcatheter, 0.032, 150cm, Back Up and Extra Back UpDQY · Special 07/03/2017SE
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Questions and answers

When was Codman * Reusable Perforator cleared by the FDA?

Codman * Reusable Perforator (K820087) received a 510(k) decision of Substantially Equivalent on February 4, 1982, 22 days after the submission was received.

What is the product code of K820087?

The FDA product code is HBF – Drills, Burrs, Trephines & Accessories (Compound, Powered), a Class II (moderate risk) device regulated under 21 CFR 882.4305.