Easydrill Autostop Cranial Perforator

FDA 510(k) K141455 · Micromar Ind. Com. , Ltd.

Substantially Equivalent

510(k) numberK141455

Submission

Device name
Easydrill Autostop Cranial Perforator
Applicant
Micromar Ind. Com. , Ltd.
Fort Worth, TX, US
Received
June 2, 2014
Decision date
March 16, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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
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
K032970Acra-Cut Xpress 120HBF · Traditional Acra Cut, Inc.12/08/2003SE

Questions and answers

When was Easydrill Autostop Cranial Perforator cleared by the FDA?

Easydrill Autostop Cranial Perforator (K141455) received a 510(k) decision of Substantially Equivalent on March 16, 2015, 287 days after the submission was received.

What is the product code of K141455?

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