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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.
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