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MedCAD secures FDA 510(k) clearance for AccuStride foot and ankle system

Summary by Medical Device Network
MedCAD has received 510(k) clearance from the US Food and Drug Administration (FDA) for its AccuStride Foot and Ankle System.The post MedCAD secures FDA 510(k) clearance for AccuStride foot and ankle system appeared first on Medical Device Network.
DisclaimerThis story is only covered by news sources that have yet to be evaluated by the independent media monitoring agencies we use to assess the quality and reliability of news outlets on our platform. Learn more here.

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Medical Device NetworkMedical Device Network

MedCAD secures FDA 510(k) clearance for AccuStride foot and ankle system

MedCAD has received 510(k) clearance from the US Food and Drug Administration (FDA) for its AccuStride Foot and Ankle System.The post MedCAD secures FDA 510(k) clearance for AccuStride foot and ankle system appeared first on Medical Device Network.

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Ortho Spine News | Your Trusted Voice for Medical Device Industry Ortho NewsOrtho Spine News | Your Trusted Voice for Medical Device Industry Ortho News

MedCAD’s AccuStride® Receives 510(k) Clearance for New Entry into Foot and Ankle Marketplace – Ortho Spine News

DALLAS, March 26, 2025 /PRNewswire/ — Dallas-based MedCAD has announced the 510(k) clearance of its AccuStride® Foot and Ankle System, making these patient-specific precision devices available to surgeons. The unique design of these devices, coupled with the company’s proprietary software, will enable foot and ankle surgeons to correct multiple related pathologies in a single procedure. The patent-pending AccuStride® System marks the company’s fi

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Ortho Spine News | Your Trusted Voice for Medical Device Industry Ortho News broke the news in on Wednesday, March 26, 2025.
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