SutureTech Gains FDA 510(k) Clearance for RapidFix

SutureTech Announces FDA 510(k) Clearance for RapidFix

SutureTech was granted FDA 510(k) clearance to market RapidFix, an All-Suture Dual Anchor System. RapidFix is intended for fixation of soft tissue to bone in a variety of orthopedic procedures. Limited launch will occur within 4Q25.

RapidFix is a 100% suture-based internal fixation device engineered to create secure tendon-to-bone repairs...

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JV

Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.



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