Centric Medical received FDA 510(k) clearance to market its SATURN external fixation system for foot, ankle and long bone segments.
This is Centric's fourth product announcement of the year; previous three include:
- The launch of ROGUE+™, a sterile-packaged hammertoe correction system.
- FDA 510(k) clearance for a new foot and ankle plating system.
- Expanded FDA 510(k) clearance for its Cannulated Screw internal fixation system in foot/ankle reconstruction.
Source: Centric Medical; ORTHOWORLD, Inc.