Exactech Receives FDA 510(k) Clearance for Vantage Total Ankle

By Julie A. Vetalice

Exactech received FDA 510(k) clearance to market the Vantage™ Total Ankle, marking its entry in the foot and ankle segment. Targeted clinical evaluation will commence during mid-2016, with full launch slated for 1Q17.

The system incorporates the press-fit bone cage design used in the Equinoxe shoulder system, developed to support initial and long-term fixation.

Source: Exactech, Inc.

Other 2016 launches planned by Exactech include:

  • Logic CC revision knee
  • An advanced bearing ceramic shoulder
  • A revision hip stem

Product Labels: Ankle Replacement

Tags: 510(k) Clearance, Regulatory