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FDA 510(k)

Tigon Medical Gryphon Anchor Line

K-Number: K220464 · 2023-03-22

ApplicantTigon Medical
Decision Date2023-03-22
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Tigon Medical Gryphon Anchor Line is a medical device manufactured by Tigon Medical. It received FDA 510(k) clearance on 2023-03-22 under approval number K220464. 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 Tigon Medical Gryphon Anchor Line?

Tigon Medical Gryphon Anchor Line is a medical device that received FDA 510(k) clearance on 2023-03-22. It is manufactured by Tigon Medical. The 510(k) number is K220464.

When was Tigon Medical Gryphon Anchor Line approved by the FDA?

Tigon Medical Gryphon Anchor Line received FDA 510(k) clearance on 2023-03-22, under approval number K220464.

What company makes Tigon Medical Gryphon Anchor Line?

Tigon Medical Gryphon Anchor Line is manufactured by Tigon Medical.

What is the FDA product code for Tigon Medical Gryphon Anchor Line?

The FDA product code for Tigon Medical Gryphon Anchor Line is MBI.

Other Devices by Tigon Medical

K182507Tigon Medical Tissue Anchors K211049Tigon Medical Button System K242529Tigon Medical All-Suture Anchors (ASA) K240175Tigon Medical Fractures, Instability, and Reconstruction (FIRE) K252596Tigon Medical Knotless and Dual Javelin All-Suture Anchors K260921Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture Anchor Line

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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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