SportLinc Receives FDA Clearance: Lincotek Targets Orthopedic OEM Market
Summary
Lincotek has obtained 510(k) clearance (K252081) from the U.S. Food and Drug Administration (FDA) for its SportLinc Syndesmosis Device, a sterile, single-use im...
Description
Lincotek has obtained 510(k) clearance (K252081) from the U.S. Food and Drug Administration (FDA) for its SportLinc Syndesmosis Device, a sterile, single-use im...
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