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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 a medical device manufactured by Conmed Corporation. It received FDA 510(k) clearance on 2017-01-25 under approval 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. It is manufactured by Conmed Corporation. The 510(k) number is K163258.

When was CrossFT Knotless Suture Anchor with Disposable Driver approved by the FDA?

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

What company makes CrossFT Knotless Suture Anchor with Disposable Driver?

CrossFT Knotless Suture Anchor with Disposable Driver is manufactured by Conmed Corporation.

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

NCT04552119 Safety of Treatment of Shoulder Repair COMPLETED NCT07491276 Efficacy of Using Knotless Barbed Suture vs N-Butyl Cyanoacrylate Glue Tissue Adhesive for Closure of Intraoral Surgical Incisions ACTIVE_NOT_RECRUITING

Related PubMed Literature

PMID: 40868376 Correlation Analysis of Suture Anchor Pull-Out Strength with Cortical Bone Thickness and Cancellous Bone Density on a Finite Element Model. Bioengineering (Basel, Switzerland) (2025)

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Related Devices (Code: MBI)

K163034SUTUREFIX Curved Suture AnchorSmith and Nephew, Inc. K162198GFS UltimateParcus Medical, LLC K162386KATOR Suture AnchorKator, LLC K161033AFX™ Femoral Implant With InserterCayenne Medical, Inc. K160996Dunamis Suture Anchor PEEK 3.0mm, 3.5mm, 4.5mm, 5.5mm, 6.5mmDunamis, LLC K161001MILAGRO ADVANCE PEEK Interference ScrewMedos International SARL

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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