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Panel Recommends Conditional Approval of TMJ Implants' Prosthetic Device

This article was originally published in The Gray Sheet

Executive Summary

TMJ Implants, Inc. should conduct a prospective, three to five-year study to gather long-term safety and efficacy data on a patient population classified according to interventional history and individual patient indication, FDA's Dental Products Panel concluded May 11 in Gaithersburg, Maryland.
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