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FDA 510(k)

MICRUS MICROCOIL DELIVERY SYSTEM

K-Number: K082739 · 2008-10-17

ApplicantMicrus Endovascular Corporation
Decision Date2008-10-17
Product CodeHCG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MICRUS MICROCOIL DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Micrus Endovascular Corporation. It received FDA 510(k) clearance on 2008-10-17 under 510(k) number K082739. The device is classified under product code HCG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRUS MICROCOIL DELIVERY SYSTEM?

MICRUS MICROCOIL DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 2008-10-17. The listed applicant is Micrus Endovascular Corporation. The 510(k) number is K082739.

When did MICRUS MICROCOIL DELIVERY SYSTEM receive FDA 510(k) clearance?

MICRUS MICROCOIL DELIVERY SYSTEM received FDA 510(k) clearance on 2008-10-17, under 510(k) number K082739.

Who is the listed applicant for MICRUS MICROCOIL DELIVERY SYSTEM?

The FDA 510(k) record lists Micrus Endovascular Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRUS MICROCOIL DELIVERY SYSTEM?

The FDA product code for MICRUS MICROCOIL DELIVERY SYSTEM is HCG.

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Other records listing Micrus Endovascular Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K103780MICRUS ASCENT OCCLUSION BALLOON CATHETER 4X7 MM; MICRUS ASCENT OCCLUSION BALLOON CATHETER 6X9 MM; MICRUS SUMMIT OCCLUSIOK102818MICRUS ONE 2 ONE GUIDEWIRE, MICRUS ONE 2 ONE SOFT GUIDEWIREK092702MICRUS MICROCATHETER, MODEL COURIER 270K091504MICRUS ASCENT OCCLUSION BALLOON CATHETER 4X7MM,6X9MM, MICRUS SUMMIT OCCLUSION BALLOON CATHETER 4X10MM,4X15, MODEL BRS 00K083922MICRUS MICROCATHETER, COURIER FLEX, MODEL MSF 170000-00K090274MICRUS ONE 2 ONE GUIDEWIRE AND SOFT GUIDEWIRE

View all 23 devices →

Related Devices (Code: HCG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262419MICRUSFRAME (MFR100202); MICRUSFRAME (MFR100253); MICRUSFRAME (MFR100305); MICRUSFRAME (MFR100356); MICRUSFRAME (MFR100407); MICRUSFRAME (MFR100412); MICRUSFRAME (MFR100509); MICRUSFRAME (MFR100517); MICRUSFRAME (MFR100611); MICRUSFRAME (MFR100626); MICRUSFRAME (MFR100713); MICRUSFRAME (MFR100730); MICRUSFRAME (MFR100816); MICRUSFRAME (MFR100829); MICRUSFRAME (MFR140225); MICRUSFRAME (MFR140303); MICRUSFRAME (MFR140304); MICRUSFRAME (MFR140306); MICRUSFRAME (MFR140406); MICRUSFRAME (MFCerenovus, Inc.K261772Target Xtra Detachable CoilStryker NeurovscularK260351Numen™ Helia Coil Embolization System; NumenFR™ Detachment SystemMicroPort NeuroTech (Shanghai) Co., Ltd.K254221Optima Coil System (OptiOne Coil System)Balt USA, LLCK252694Target Detachable CoilStryker NeurovascularK251832InZone IST Detachment System; IZDS Connecting CableStryker Neurovascular

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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