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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 the device name listed in this FDA 510(k) record. The listed applicant is Tigon Medical. It received FDA 510(k) clearance on 2023-03-22 under 510(k) 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. The listed applicant is Tigon Medical. The 510(k) number is K220464.

When did Tigon Medical Gryphon Anchor Line receive FDA 510(k) clearance?

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

Who is the listed applicant for Tigon Medical Gryphon Anchor Line?

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

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 records listing Tigon Medical 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.

K260921Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture Anchor LineK252596Tigon Medical Knotless and Dual Javelin All-Suture AnchorsK242529Tigon Medical All-Suture Anchors (ASA)K240175Tigon Medical Fractures, Instability, and Reconstruction (FIRE)K211049Tigon Medical Button SystemK182507Tigon Medical Tissue Anchors

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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.

K262047Grappler Suture Anchor SystemParagon 28, Inc.K262369AIR+ All-Inside Meniscal Repair Device, Curved Up;AIR+ All-Inside Meniscal Repair Device, Curved DownStryker EndoscopyK261770Suture Button Repair SystemSkeletal Dynamics, Inc.K261632Thunderbolt SystemResponsive Arthroscopy, Inc.K261968Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one black knotless and one blue MINITAPE suture (72205981); Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one blue knotless and one black MINITAPE suture (72205982)Smith & Nephew, Inc.K260018Arthrex FiberButtonArthrex, Inc.

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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