FDA 510(k) Applications Submitted by LYNETTE WHITAKER

FDA 510(k) Number Submission Date Device Name Applicant
K960278 01/19/1996 COBALT-CHROMIUM-MOLYBDENUM (CO-CR-MO) ALLOY FEMORAL HEADS W/CO-NIDIUM SURFACE TREATMENT ZIMMER, INC.
K961789 05/09/1996 RESORBABLE SOFT TISSUE ATTACHMENT DEVICE ZIMMER, INC.
K982320 07/02/1998 DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM DEPUY, INC.
K032398 08/04/2003 PLUS PIVOT LINK UNIVERSAL SYSTEM SPINEVISION, INC.
K983583 10/13/1998 DEPUY ACROMED MOSS AND MOSS MIAMI SPINAL SYSTEMS DEPUY, INC.
K042930 10/22/2004 SPACEVISION CAGE SYSTEM SPINEVISION, INC.


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