FDA Clears Trax Surgical’s Linkt Nitinol Compression Staple System
Trax Surgical announced FDA 510(k) clearance for its Linkt Compression Staple System, designed for fracture repair, joint fusion, and osteotomy procedures. The system offers a
Trax Surgical announced FDA 510(k) clearance for its Linkt Compression Staple System, designed for fracture repair, joint fusion, and osteotomy procedures. The system offers a
Medtronic (NYSE: MDT) anticipates tariffs imposed by the U.S. and reciprocal tariffs abroad will cost the company between $200 million and $350 million in its
Stryker announced FDA 510(k) clearance for its OptaBlate BVN system, designed to provide targeted, minimally invasive treatment for chronic vertebrogenic low back pain. The system
Philips has initiated the RADIQAL (radiation dose and image quality) trial, a multicenter, randomized study enrolling 824 patients with coronary artery disease across six hospitals
Route 92 Medical announced FDA 510(k) clearance for its HiPoint reperfusion system, featuring the super-bore .088” HiPoint 88 aspiration catheter and the Monopoint approach. This
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