Exactech Reports the US FDA 510(k) Clearance of ExactechGPS Ankle as a Surgical Navigation System for Total Ankle Replacement
Shots:
- BlueOrtho a subsidiary of Exactech received the US FDA’s 510(k) clearance for ExactechGPS Ankle, a surgical navigation system for total ankle arthroplasty (TAA)
- The pre-clinical analysis of the GPS Ankle system depicted an accuracy of 2mm & 2 degrees relative to CT-based surgical plans, further confirmed by two studies on sawbones, recently accepted by the Orthopaedic Research Society
- ExactechGPS Ankle system uses a compact touchscreen tablet & proprietary active tracker technology to connect preoperative plans with real-time instrument guidance, confirming the resection site according to surgical plan. The system is compatible with the company’s Vantage Total Ankle System
Ref: Exactech | Image: Exactech
Related News:- Exactech Acquires Muvr and it's Digital Health Tech for Orthopedic Practices
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Kritika is a content writer at PharmaShots. She is interested in covering recent innovations from the pharma & MedTech industry. She covers news related to Product approvals, clinical trial results, and updates. She can be contacted at connect@pharmashots.com.
