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FDA 510(k)

MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01

K-Number: K022420 · 2002-10-22

ApplicantMicrus Corp.
Decision Date2002-10-22
Product CodeHCG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01 is the device name listed in this FDA 510(k) record. The listed applicant is Micrus Corp.. It received FDA 510(k) clearance on 2002-10-22 under 510(k) number K022420. 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 STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01?

MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01 is a medical device that received FDA 510(k) clearance on 2002-10-22. The listed applicant is Micrus Corp.. The 510(k) number is K022420.

When did MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01 receive FDA 510(k) clearance?

MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01 received FDA 510(k) clearance on 2002-10-22, under 510(k) number K022420.

Who is the listed applicant for MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01?

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

What is the FDA product code for MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01?

The FDA product code for MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01 is HCG.

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Other records listing Micrus Corp. 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.

K033813MICRUS MODIFIED MICROCOIL SYSTEM, CERECYTEK032872MICRUS MICROCOIL SYSTEMK032624MICRUS MICROCATHETERK031578MICRUS MICROCOIL SYSTEMS, MODELS HEL, SPH, STR, FSR AND HSRK002056MICRUS MICROCOIL DELIVERY SYSTEM, MDS03

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

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

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