WebDevice Classification Name: filler, bone void, calcium compound: 510(k) Number: K200064: Device Name: OsteoFlo NanoPutty-Quadphasic Synthetic Bone Graft WebFood and Drug Administration

SurGenTec® Announces FDA Clearance for OsteoFlo® …

WebAugust 26, 2024 BOCA RATON, Fla.–(BUSINESS WIRE)–SurGenTec, a privately held spine and orthopedic technology company, announced today that it has received 510(k) … WebThe following data is part of a premarket notification filed by Surgentec, Llc with the FDA for Osteoflo Nanoputty-quadphasic Synthetic Bone Graft. Pre-market Notification Details. Device ID: K200064: 510k Number: K200064: Device Name: OsteoFlo NanoPutty-Quadphasic Synthetic Bone Graft: buddy ryan past teams coached

OsteoFlo NanoPutty-Quadphasic Synthetic Bone Graft

WebAug 27, 2024 · BOCA RATON, Fla.–(BUSINESS WIRE)–SurGenTec, a privately held spine and orthopedic technology company, announced today that it has received 510(k) clearance … WebAug 26, 2024 · BOCA RATON, Fla.--(BUSINESS WIRE)-- SurGenTec, a privately held spine and orthopedic technology company, announced today that it has received 510(k) clearance … WebThe following data is part of a premarket notification filed by Surgentec, Llc with the FDA for Osteoflo Nanoputty-quadphasic Synthetic Bone Graft. Pre-market Notification Details. … buddy ryan punches kevin gilbride