Paritic Inc´s navigation system received FDA´s 510(k) clearance
27/11/2014view : 4649

New York,New,York;Jun 28, 2014. The surgical navigation system, Pari-Path, developed by Paritic Inc was cleared by FDA for 510(k) on Jun 27, 2014.

The Pari-Path navigation system displays the simulated image of an interventional instrument (a tracked insertion tool), such as a biopsy needle, an ablation needle, or probe, on a computer monitor screen that presents an image model of the target organs and the current and the projected future path of the interventional instrument.

The system is intended for treatment planning and intra-operative guidance for surgical procedures.

Paritic Inc is now working on marketing the navigation device and looking for various partners.