Artoss announced FDA 510(k) clearance to market NanoBone® SBX Putty.
NanoBone synthetic bone graft products have been used in Europe for ten years in nearly 400,000 clinical cases, across all indications. The newly-cleared product is exclusively distributed in North America by Artoss Inc., which launched the company’s NanoBone Granule product in 2015.
Source: Artoss, Inc.
Artoss announced FDA 510(k) clearance to market NanoBone® SBX Putty.
NanoBone synthetic bone graft products have been used in Europe for ten years in nearly 400,000 clinical cases, across all indications. The newly-cleared product is exclusively...
Artoss announced FDA 510(k) clearance to market NanoBone® SBX Putty.
NanoBone synthetic bone graft products have been used in Europe for ten years in nearly 400,000 clinical cases, across all indications. The newly-cleared product is exclusively distributed in North America by Artoss Inc., which launched the company’s NanoBone Granule product in 2015.
Source: Artoss, Inc.
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