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The clearance allows for the marketing of the device in the United States.
TriSalus Life Sciences, Inc. (Nasdaq: TLSI) announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for its TriNav Advance Delivery Device. This clearance permits the company to market the device for use in the United States.
The TriNav Advance Delivery Device is designed to enhance the delivery of therapeutic agents directly to target tissues, improving treatment efficacy and patient outcomes. With a free float of 38,159,873 shares, TriSalus Life Sciences continues to expand its product offerings in the medical devices sector.
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