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

By Julie A. Vetalice

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.

Product Labels: External Fixation

Tags: 510(k) Clearance, Regulatory