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FDA 510(k)

OSSIO™ Pin Product Family

K-Number: K181180 · 2019-01-10

ApplicantOSSIO , Ltd.
Decision Date2019-01-10
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSSIO™ Pin Product Family is a medical device manufactured by OSSIO , Ltd.. It received FDA 510(k) clearance on 2019-01-10 under approval number K181180. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSSIO™ Pin Product Family?

OSSIO™ Pin Product Family is a medical device that received FDA 510(k) clearance on 2019-01-10. It is manufactured by OSSIO , Ltd.. The 510(k) number is K181180.

When was OSSIO™ Pin Product Family approved by the FDA?

OSSIO™ Pin Product Family received FDA 510(k) clearance on 2019-01-10, under approval number K181180.

What company makes OSSIO™ Pin Product Family?

OSSIO™ Pin Product Family is manufactured by OSSIO , Ltd..

What is the FDA product code for OSSIO™ Pin Product Family?

The FDA product code for OSSIO™ Pin Product Family is HTY.

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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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