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FDA 510(k)

KISSloc Suture System

K-Number: K170440 · 2017-05-03

ApplicantArthrosurface, Inc.
Decision Date2017-05-03
Product CodeHTN
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KISSloc Suture System is a medical device manufactured by Arthrosurface, Inc.. It received FDA 510(k) clearance on 2017-05-03 under approval number K170440. The device is classified under product code HTN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KISSloc Suture System?

KISSloc Suture System is a medical device that received FDA 510(k) clearance on 2017-05-03. It is manufactured by Arthrosurface, Inc.. The 510(k) number is K170440.

When was KISSloc Suture System approved by the FDA?

KISSloc Suture System received FDA 510(k) clearance on 2017-05-03, under approval number K170440.

What company makes KISSloc Suture System?

KISSloc Suture System is manufactured by Arthrosurface, Inc..

What is the FDA product code for KISSloc Suture System?

The FDA product code for KISSloc Suture System is HTN.

Related Clinical Trials

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Other Devices by Arthrosurface, Inc.

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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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