In my case, there are regulations that apply to individuals that are covered under the Federal Employee Health Benefits plan, so they may not be applicable in your case. Simply put, FEHB carriers are not allowed to classify a FDA-approved device as experimental, which is exactly what MD-IPA did - twice.
Laura, do you have any info on actual vs theoretical advantages of the coated endplates?
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Stan
L5-S1 DDD and herniation
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