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FDA 510(k)

VersaLoop Anchor System

K-Number: K202178 · 2020-11-13

ApplicantT.A.G. Medical Products Corporation, Ltd.
Decision Date2020-11-13
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VersaLoop Anchor System is a medical device manufactured by T.A.G. Medical Products Corporation, Ltd.. It received FDA 510(k) clearance on 2020-11-13 under approval number K202178. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VersaLoop Anchor System?

VersaLoop Anchor System is a medical device that received FDA 510(k) clearance on 2020-11-13. It is manufactured by T.A.G. Medical Products Corporation, Ltd.. The 510(k) number is K202178.

When was VersaLoop Anchor System approved by the FDA?

VersaLoop Anchor System received FDA 510(k) clearance on 2020-11-13, under approval number K202178.

What company makes VersaLoop Anchor System?

VersaLoop Anchor System is manufactured by T.A.G. Medical Products Corporation, Ltd..

What is the FDA product code for VersaLoop Anchor System?

The FDA product code for VersaLoop Anchor System is MBI.

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Other Devices by T.A.G. Medical Products Corporation, Ltd.

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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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