Centric Medical Gains FDA 510(k) Clearance for SATURN External Fixation System

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...

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Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.

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