Surmodics Receives FDA 510(k) Clearance For Pounce XL Thrombectomy System
Portfolio Pulse from Benzinga Newsdesk
Surmodics has received FDA 510(k) clearance for its Pounce XL Thrombectomy System. The company plans a limited market release in the first half of 2025, followed by full commercialization.
October 01, 2024 | 11:08 am
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Surmodics received FDA 510(k) clearance for its Pounce XL Thrombectomy System, indicating regulatory approval for market entry. A limited market release is planned for the first half of 2025, with full commercialization to follow.
The FDA 510(k) clearance is a significant regulatory milestone for Surmodics, allowing them to proceed with market entry plans. This clearance is likely to positively impact investor sentiment and the stock price in the short term, as it paves the way for future revenue generation through the planned commercialization of the Pounce XL Thrombectomy System.
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