FDA 510(k) Applications Submitted by REBECCA LENNARD

FDA 510(k) Number Submission Date Device Name Applicant
K062352 08/11/2006 FRS SCREW DEPUY ORTHOPAEDICS, INC.
K063652 12/08/2006 GLOBAL AP POROUS COATED HUMERAL STEM DEPUY ORTHOPAEDICS, INC.
K063686 12/12/2006 DEPUY LPS DISTAL FEMORAL COMPONENT DEPUY ORTHOPAEDICS, INC.
K040644 03/11/2004 MODIFICATION TO DEPUY CERAMIC FEMORAL HEAD DEPUY ORTHOPAEDICS, INC.


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