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FDA 510(k)

ZUMA

K-Number: K071726 · 2007-10-23

ApplicantSeaspine, Inc.
Decision Date2007-10-23
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ZUMA is the device name listed in this FDA 510(k) record. The listed applicant is Seaspine, Inc.. It received FDA 510(k) clearance on 2007-10-23 under 510(k) number K071726. 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 ZUMA?

ZUMA is a medical device that received FDA 510(k) clearance on 2007-10-23. The listed applicant is Seaspine, Inc.. The 510(k) number is K071726.

When did ZUMA receive FDA 510(k) clearance?

ZUMA received FDA 510(k) clearance on 2007-10-23, under 510(k) number K071726.

Who is the listed applicant for ZUMA?

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

What is the FDA product code for ZUMA?

The FDA product code for ZUMA is MQP.

Other records listing Seaspine, Inc. 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.

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