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Pro Osteon Bone Void Filler Study — PO  

Osteoarthritis Clinical Trial

Official title:
Pro Osteon Bone Void Filler Data Collection

Clinical Trial Summary

This study was designed to observe the outcomes of Pro Osteon according to its cleared indications for use.

Clinical Trial Description

The purpose of this prospective clinical data-collection is to document the performance and clinical outcomes of Pro Osteon® as a Bone Void Filler. FDA has cleared this device via premarket notifications 510(k) K063346, K980817, and K990131. There will be no experimental or investigational devices used. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00858598
Study type Observational
Source Zimmer Biomet
Contact
Status Withdrawn
Phase N/A
Start date December 2009
Completion date January 2014
View Details
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