FDA 510(k) Applications Submitted by DOUGLAS W STUART

FDA 510(k) Number Submission Date Device Name Applicant
K954186 09/06/1995 SLED UNICOMPARTMENT KNEE SYSTEM LINK AMERICA, INC.
K970084 01/09/1997 LINK CERCLAGE WIRE SYSTEM TURNKEY INTERGRATION USA, INC.
K990523 02/19/1999 B2C, ESPACE REVISION CUP SYSTEM TURNKEY INTERGRATION USA, INC.
K991405 04/22/1999 OMNI-FIX, HUMERAL NAIL TURNKEY INTERGRATION USA, INC.
K961899 05/16/1996 CPS, CEMENTED HIP SYSTEM ARTOS MEDICAL PRODUCTS GMBH
K962034 05/24/1996 SC, CEMENTLESS HIP SYSTEM ARTOS MEDICAL PRODUCTS GMBH
K962086 05/29/1996 CPS, CEMENTED CUP SYSTEM ARTOS MEDICAL PRODUCTS GMBH
K991962 06/10/1999 EIS DYNAMIC MEMORY STAPLES SYSTEM GROUPE LEPINE
K991964 06/10/1999 EIS THREADED SCREW FRACTURE FIXATION GROUPE LEPINE
K962268 06/13/1996 CHROME COBALT BALL HEAD ARTOS MEDICAL PRODUCTS GMBH
K972411 06/26/1997 LINK CEMENT PLUG TURNKEY INTERGRATION USA, INC.
K972760 07/24/1997 LINK, ACETABULAR REVISION MESH CUP LINK AMERICA, INC.
K992490 07/26/1999 B2C HIP SYSTEM LEPINE GROUPE SPA.
K993713 11/03/1999 RIM-FIX, ACETABULAR CUP SURGICAL IMPLANTS INC.
K964458 11/07/1996 ELLIS EXTERNAL MINI-FIXATOR SYSTEM LINK AMERICA, INC.
K955296 11/16/1995 LINK MP RECONSTRUCTION HIP LINK AMERICA, INC.


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