Smith+Nephew Announces FDA 510(k) Clearance For Its New CATALYSTEM Primary Hip System
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Smith+Nephew has received FDA 510(k) clearance for its new CATALYSTEM Primary Hip System, which is expected to enhance its product offerings in the orthopedic market.

July 16, 2024 | 12:14 pm
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Smith+Nephew has received FDA 510(k) clearance for its new CATALYSTEM Primary Hip System, which is expected to enhance its product offerings in the orthopedic market.
The FDA 510(k) clearance is a significant regulatory milestone that allows Smith+Nephew to market its new CATALYSTEM Primary Hip System in the US. This is likely to enhance its product portfolio and potentially increase market share in the orthopedic sector.
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