FDA 510(k)

CURIOS

K-Number: K090641 · 2009-10-23

Decision Date2009-10-23

Product CodeMQV

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

CURIOS is the device name listed in this FDA 510(k) record. The listed applicant is Progentix Orthobiology BV. It received FDA 510(k) clearance on 2009-10-23 under 510(k) number K090641. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURIOS?

CURIOS is a medical device that received FDA 510(k) clearance on 2009-10-23. The listed applicant is Progentix Orthobiology BV. The 510(k) number is K090641.

When did CURIOS receive FDA 510(k) clearance?

CURIOS received FDA 510(k) clearance on 2009-10-23, under 510(k) number K090641.

Who is the listed applicant for CURIOS?

The FDA 510(k) record lists Progentix Orthobiology BV as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CURIOS?

The FDA product code for CURIOS is MQV.

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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.