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PMCF Study on PEEK Suture Anchors for Shoulder Indications

NCT03826667 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 464

Last updated 2022-04-12

Study results available
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Summary

Post-market clinical follow-up on the PEEK Suture Anchors in the shoulder.

Conditions

  • Soft Tissue to Bone Fixation

Interventions

DEVICE

Polyetheretherketone (PEEK) Shoulder Suture Anchors

PEEK Suture Anchors, which include: * HEALICOIL™ PK Preloaded Suture Anchors * BIORAPTOR™ 2.3 PK Suture Anchors/BIORAPTOR™ Curved 2.3 PK Suture Anchors * BIORAPTOR™ Knotless Suture Anchors * MULTIFIX™ S Ultra Knotless Fixation System * FOOTPRINT™ Ultra PK Suture Anchors * TWINFIX™ Ultra PK Suture Anchors/TWINFIX™ Ultra Preloaded and with Needles * SPEEDSCREW™ Knotless Fixation System * SpeedLock Knotless Fixation Device

Sponsors & Collaborators

  • Smith & Nephew, Inc.

    lead INDUSTRY

Principal Investigators

  • Judth Horner · Smith & Nephew, Inc.

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-14
Primary Completion
2019-08-28
Completion
2019-08-28

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03826667 on ClinicalTrials.gov