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In Brief: FDA Orthopedic and Rehabilitation Devices Panel

This article was originally published in The Gray Sheet

Executive Summary

FDA Orthopedic and Rehabilitation Devices Panel: Jan. 12 meeting at FDA's Parklawn Building in Rockville, Maryland, will address reclassification petitions for non- and semi-constrained shoulders and uni- and total-patellofemorotibial knees. On Jan. 13, the advisory committee will discuss petitions on patellofemoral knees and constrained elbows, as well as classification of calcium sulfate pre-formed pellets (plaster of paris pellets). Written submissions for presentation at the meeting are due by Jan. 5; for more information contact panel secretary Jodi Nashman at 301/594-2036...

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