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Celularity Receives U S Food And Drug Administration (FDA) Preliminary Assessment For Celularity s Investigational Fuse Bone Void Filler To Be Regulated As A Device By FDA s Center For Devices And Radiological Health
Celularity’s Pre-Request for Designation is based on data demonstrating 100 percent biochemical characterization of the product Celularity intends to submit 510 pre-market notification to the. | April 3, 2023
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