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FDA 510(k)

CrossFT Knotless Suture Anchor with Disposable Driver

K-Number: K163258 · 2017-01-25

ApplicantConmed Corporation
Decision Date2017-01-25
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CrossFT Knotless Suture Anchor with Disposable Driver is the device name listed in this FDA 510(k) record. The listed applicant is Conmed Corporation. It received FDA 510(k) clearance on 2017-01-25 under 510(k) number K163258. 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 CrossFT Knotless Suture Anchor with Disposable Driver?

CrossFT Knotless Suture Anchor with Disposable Driver is a medical device that received FDA 510(k) clearance on 2017-01-25. The listed applicant is Conmed Corporation. The 510(k) number is K163258.

When did CrossFT Knotless Suture Anchor with Disposable Driver receive FDA 510(k) clearance?

CrossFT Knotless Suture Anchor with Disposable Driver received FDA 510(k) clearance on 2017-01-25, under 510(k) number K163258.

Who is the listed applicant for CrossFT Knotless Suture Anchor with Disposable Driver?

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

What is the FDA product code for CrossFT Knotless Suture Anchor with Disposable Driver?

The FDA product code for CrossFT Knotless Suture Anchor with Disposable Driver is MBI.

Related Clinical Trials

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.

NCT04552119Safety of Treatment of Shoulder RepairCOMPLETED

Other records listing Conmed Corporation 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.

K261363Y-Knotless™ Flex AnchorsK253763Y-Knotless™ Flex AnchorsK252946BioBrace® Extra-Articular Ligament Augmentation KitK251530CONMED Argo Knotless® AnchorK250395BioBrace ® RC Delivery SystemK244025Argo Knotless GENESYS Anchor

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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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