FDA 510(k)

NEXUS DETACHABLE COIL SYSTEM, MORPHEUS 3D CSR

K-Number: K060625 · 2006-04-20

Decision Date2006-04-20

Product CodeHCG

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

NEXUS DETACHABLE COIL SYSTEM, MORPHEUS 3D CSR is the device name listed in this FDA 510(k) record. The listed applicant is Micro Therapeutics, Inc.. It received FDA 510(k) clearance on 2006-04-20 under 510(k) number K060625. 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 NEXUS DETACHABLE COIL SYSTEM, MORPHEUS 3D CSR?

NEXUS DETACHABLE COIL SYSTEM, MORPHEUS 3D CSR is a medical device that received FDA 510(k) clearance on 2006-04-20. The listed applicant is Micro Therapeutics, Inc.. The 510(k) number is K060625.

When did NEXUS DETACHABLE COIL SYSTEM, MORPHEUS 3D CSR receive FDA 510(k) clearance?

NEXUS DETACHABLE COIL SYSTEM, MORPHEUS 3D CSR received FDA 510(k) clearance on 2006-04-20, under 510(k) number K060625.

Who is the listed applicant for NEXUS DETACHABLE COIL SYSTEM, MORPHEUS 3D CSR?

The FDA 510(k) record lists Micro Therapeutics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEXUS DETACHABLE COIL SYSTEM, MORPHEUS 3D CSR?

The FDA product code for NEXUS DETACHABLE COIL SYSTEM, MORPHEUS 3D CSR is HCG.

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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.