FDA 510(k) Applications Submitted by GLOBAL ORTHOPAEDIC TECHNOLOGY, USA, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K050473 02/24/2005 RBK PATELLA FEMORAL KNEE GLOBAL ORTHOPAEDIC TECHNOLOGY, USA, INC.
K051721 06/27/2005 GLOBAL RESURFACING UNICOMPARTMENTAL KNEE SYSTEM GLOBAL ORTHOPAEDIC TECHNOLOGY, USA, INC.
K033351 10/20/2003 GLOBAL RESURFACING UNICOMPARTMENTAL (GRU) KNEE GLOBAL ORTHOPAEDIC TECHNOLOGY, USA, INC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact