FDA 510(k) Applications Submitted by TEKNIMED SA

FDA 510(k) Number Submission Date Device Name Applicant
K031826 06/13/2003 TRIHA + TEKNIMED SA
K043593 12/29/2004 SPINE-FIX BIOMIMETIC BONE CEMENT TEKNIMED SA
K090435 02/19/2009 VERTECEM TEKNIMED SA
K040669 03/15/2004 CERAFORM BONE VOID FILLER TEKNIMED SA
K080873 03/31/2008 OPACITY + BONE CEMENT TEKNIMED SA
K041493 06/04/2004 CEMENTEK TEKNIMED SA
K062102 07/24/2006 ODONCER TEKNIMED SA
K032685 08/29/2003 CEMSTOP CEMENT RESTRICTOR TEKNIMED SA
K083005 10/08/2008 NANGEL TEKNIMED SA
K042911 10/21/2004 CEMENTEK LV TEKNIMED SA
K103433 11/24/2010 F20 TEKNIMED SA


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