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FDA 510(k)

VersaLoop Anchor System

K-Number: K202178 · 2020-11-13

Decision Date2020-11-13
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VersaLoop Anchor System is the device name listed in this FDA 510(k) record. The listed applicant is T.A.G. Medical Products Corporation, Ltd.. It received FDA 510(k) clearance on 2020-11-13 under 510(k) 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. The listed applicant is T.A.G. Medical Products Corporation, Ltd.. The 510(k) number is K202178.

When did VersaLoop Anchor System receive FDA 510(k) clearance?

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

Who is the listed applicant for VersaLoop Anchor System?

The FDA 510(k) record lists T.A.G. Medical Products Corporation, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VersaLoop Anchor System?

The FDA product code for VersaLoop Anchor System is MBI.

Other records listing T.A.G. Medical Products Corporation, Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 7 devices →

Related Devices (Code: MBI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.