FDA 510(k)

MICRUS MICROCOIL SYSTEM, CASHMERE MODEL SRC

K-Number: K063653 · 2007-01-17

ApplicantMicrus Endovascular Corporation

Decision Date2007-01-17

Product CodeHCG

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MICRUS MICROCOIL SYSTEM, CASHMERE MODEL SRC 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 2007-01-17 under 510(k) number K063653. 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 SYSTEM, CASHMERE MODEL SRC?

MICRUS MICROCOIL SYSTEM, CASHMERE MODEL SRC is a medical device that received FDA 510(k) clearance on 2007-01-17. The listed applicant is Micrus Endovascular Corporation. The 510(k) number is K063653.

When did MICRUS MICROCOIL SYSTEM, CASHMERE MODEL SRC receive FDA 510(k) clearance?

MICRUS MICROCOIL SYSTEM, CASHMERE MODEL SRC received FDA 510(k) clearance on 2007-01-17, under 510(k) number K063653.

Who is the listed applicant for MICRUS MICROCOIL SYSTEM, CASHMERE MODEL SRC?

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 SYSTEM, CASHMERE MODEL SRC?

The FDA product code for MICRUS MICROCOIL SYSTEM, CASHMERE MODEL SRC is HCG.

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Other records listing Micrus Endovascular Corporation as applicant

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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.