Osteoarthritis Clinical Trial
Official title:
Pro Osteon Bone Void Filler Data Collection
This study was designed to observe the outcomes of Pro Osteon according to its cleared indications for use.
The purpose of this prospective clinical data-collection is to document the performance and clinical outcomes of Pro Osteon® as a Bone Void Filler. FDA has cleared this device via premarket notifications 510(k) K063346, K980817, and K990131. There will be no experimental or investigational devices used. ;
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