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FDA 510(k)

MODIFICATION TO VERTE-STACK

K-Number: K040422 · 2004-03-19

ApplicantMedtronic Sofamor Danek
Decision Date2004-03-19
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO VERTE-STACK is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Sofamor Danek. It received FDA 510(k) clearance on 2004-03-19 under 510(k) number K040422. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO VERTE-STACK?

MODIFICATION TO VERTE-STACK is a medical device that received FDA 510(k) clearance on 2004-03-19. The listed applicant is Medtronic Sofamor Danek. The 510(k) number is K040422.

When did MODIFICATION TO VERTE-STACK receive FDA 510(k) clearance?

MODIFICATION TO VERTE-STACK received FDA 510(k) clearance on 2004-03-19, under 510(k) number K040422.

Who is the listed applicant for MODIFICATION TO VERTE-STACK?

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

What is the FDA product code for MODIFICATION TO VERTE-STACK?

The FDA product code for MODIFICATION TO VERTE-STACK is MQP.

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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.

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