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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 the device name listed in this FDA 510(k) record. The listed applicant is OSSIO , Ltd.. It received FDA 510(k) clearance on 2019-01-10 under 510(k) 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. The listed applicant is OSSIO , Ltd.. The 510(k) number is K181180.

When did OSSIO™ Pin Product Family receive FDA 510(k) clearance?

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

Who is the listed applicant for OSSIO™ Pin Product Family?

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

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

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

Other records listing OSSIO , Ltd. as applicant

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Related Devices (Code: 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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