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FDA 510(k)

CLAVIS

K-Number: K062478 · 2007-02-08

ApplicantMedtronic A/S
Decision Date2007-02-08
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CLAVIS is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic A/S. It received FDA 510(k) clearance on 2007-02-08 under 510(k) number K062478. The device is classified under product code BXN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLAVIS?

CLAVIS is a medical device that received FDA 510(k) clearance on 2007-02-08. The listed applicant is Medtronic A/S. The 510(k) number is K062478.

When did CLAVIS receive FDA 510(k) clearance?

CLAVIS received FDA 510(k) clearance on 2007-02-08, under 510(k) number K062478.

Who is the listed applicant for CLAVIS?

The FDA 510(k) record lists Medtronic A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLAVIS?

The FDA product code for CLAVIS is BXN.

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Related Devices (Code: BXN)

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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.

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