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Business · 28/03/2007Updated: 10/17/2026 · 1 min read

FDA Determines Regulatory Review Period for INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE Patent Extension

Summary

The US Food and Drug Administration (FDA) has officially set a regulatory review period for the INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE, a medical device, in order to extend its patents, as required by law.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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