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FDA 510(k)

MODIFICATION TO VERTE-STACK SPINAL SYSTEM

K-Number: K062133 · 2006-09-26

ApplicantMedtronic Spinal and Biologics Div
Decision Date2006-09-26
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO VERTE-STACK SPINAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Spinal and Biologics Div. It received FDA 510(k) clearance on 2006-09-26 under 510(k) number K062133. 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 SPINAL SYSTEM?

MODIFICATION TO VERTE-STACK SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 2006-09-26. The listed applicant is Medtronic Spinal and Biologics Div. The 510(k) number is K062133.

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

MODIFICATION TO VERTE-STACK SPINAL SYSTEM received FDA 510(k) clearance on 2006-09-26, under 510(k) number K062133.

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

The FDA 510(k) record lists Medtronic Spinal and Biologics Div as the applicant. This does not by itself establish the device manufacturer.

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

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

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Related Devices (Code: MQP)

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.

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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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