Medical applications developer Meridian Technique of Hampshire, U.K., has received U.S. Food and Drug Administration 510(k) pre-market clearance for its OrthoView digital templating software.
The product provides surgeons with access to a library of digital product templates and anatomical planning guides developed in conjunction with the orthopedic implant manufacturers. The templates provide a flexible and adaptable preoperative planning tool specifically for use in a PACS environment, according to Meridian.
The digital planning record is then saved for future reference, forming part of the electronic patient record, said the company.
By AuntMinnie.com staff writersSeptember 23, 2003
Copyright © 2003 AuntMinnie.com
