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FDA 510(k)

ICONIX TT All Suture Anchor

K-Number: K170098 · 2017-03-31

ApplicantStryker
Decision Date2017-03-31
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ICONIX TT All Suture Anchor is a medical device manufactured by Stryker. It received FDA 510(k) clearance on 2017-03-31 under approval number K170098. 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 ICONIX TT All Suture Anchor?

ICONIX TT All Suture Anchor is a medical device that received FDA 510(k) clearance on 2017-03-31. It is manufactured by Stryker. The 510(k) number is K170098.

When was ICONIX TT All Suture Anchor approved by the FDA?

ICONIX TT All Suture Anchor received FDA 510(k) clearance on 2017-03-31, under approval number K170098.

What company makes ICONIX TT All Suture Anchor?

ICONIX TT All Suture Anchor is manufactured by Stryker.

What is the FDA product code for ICONIX TT All Suture Anchor?

The FDA product code for ICONIX TT All Suture Anchor is MBI.

Related Clinical Trials

NCT05362370 Stryker PEEK Customized Implant: A Prospective Post Market Follow Up to Evaluate Safety, Performance and Effectiveness ACTIVE_NOT_RECRUITING NCT06941558 The UK ADAPTIS Study ACTIVE_NOT_RECRUITING NCT07245758 Facial iD Customized Mandible Reconstruction Plates COMPLETED NCT07245719 Stryker Universal Midface and Upper-Face Fixation System: A Retrospective Post Market Follow Up COMPLETED NCT07245810 Stryker Facial iD Universal Plate Configurator: A Retrospective Post Market Follow Up ACTIVE_NOT_RECRUITING NCT07221916 Stryker's Surgeon iD Mandible Reconstruction Plates: A Retrospective Post Market Follow Up COMPLETED

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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