Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Clinical Trial

MDR - Biomet Cannulated Screws

NCT: NCT04002518 · ACTIVE_NOT_RECRUITING

NCT IDNCT04002518
StatusACTIVE_NOT_RECRUITING
Start Date2019-08-07
Completion2026-10
SponsorZimmer Biomet (INDUSTRY)
First posted
Last updated

Brief Summary

The objective of this retrospective enrollment/prospective follow up study is to collect data confirming safety, performance, and clinical benefits of the Biomet Cannulated Bone Screw System (Implants and Instrumentation) when used according to the approved Indications for Use (IFU).

Frequently Asked Questions

What is MDR - Biomet Cannulated Screws?

MDR - Biomet Cannulated Screws is a clinical trial registered under NCT04002518. Current status: ACTIVE_NOT_RECRUITING.

What is the status of NCT04002518?

The current status of NCT04002518 (MDR - Biomet Cannulated Screws) is: ACTIVE_NOT_RECRUITING.

When did MDR - Biomet Cannulated Screws start?

MDR - Biomet Cannulated Screws started on 2019-08-07.

Related Devices

K193214WasherLoc and No-Profile Screw and Washer Systems, Biomet Cannulated Screw System, Biomet Headless Compression and Twist-Off ScrewsBiomet, Inc. K160058Biomet Variable Pitch Compression Screw SystemBiomet, Inc. K172408Biomet Bone Cement RBiomet, Inc. K190035Biomet Headless Compression and Twist-Off ScrewsBiomet, Inc. K243571Trabecular Metal Acetabular Revision System, Acetabular Liners and Constrained LinersZimmer Biomet

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

↑