FDA 510(k) Applications Submitted by LYNNETTE WHITAKER

FDA 510(k) Number Submission Date Device Name Applicant
K980368 01/30/1998 DEPUY MOTECH PEAK 3MM FIXATION ROD SYSTEM DEPUY, INC.
K000306 02/01/2000 PINNACLE ACETABULAR SYSTEM DEPUY ORTHOPAEDICS, INC.
K980447 02/05/1998 DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM DEPUY ORTHOPAEDICS, INC.
K030526 02/19/2003 PEDIGUARD NERVE DETECTOR SYSTEM SPINEVISION, INC.
K000658 02/28/2000 ERS RADIAL HEAD REPLACEMENT DEPUY ORTHOPAEDICS, INC.
K971144 03/28/1997 MULTITAK SS SUTURE SYSTEM BONUTTI RESEARCH
K011048 04/06/2001 BSM BONE SUBSTITUTE MATERIAL DEPUY ORTHOPAEDICS, INC.
K021507 05/09/2002 PLUS PIVOT LINK UNIVERSAL SYSTEM SPINE VISION, INC
K021510 05/09/2002 UNI-T UNI-THREAD SPINAL SYSTEM SPINE VISION, INC
K001534 05/17/2000 PINNACLE ACETABULAR SYSTEM DEPUY ORTHOPAEDICS, INC.
K011533 05/18/2001 DEPUY FEMORAL HEADS DEPUY ORTHOPAEDICS, INC.
K982011 06/08/1998 DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM DEPUY ORTHOPAEDICS, INC.
K962397 06/21/1996 STATAK SOFT TISSUE ATTACHMENT DEVICE ZIMMER, INC.
K022271 07/13/2002 PLUS PIVOT LINK UNIVERSAL SYSTEM SPINEVISION, INC.
K963109 08/12/1996 HERITAGE HIP SYSTEM ZIMMER, INC.
K973015 08/13/1997 MULTITAK SS SUTURE SYSTEM BONUTTI RESEARCH
K052406 09/01/2005 UNI-THREAD SPINAL SYSTEM SPINE VISION, INC
K042640 09/27/2004 UNI-THREAD SPINAL SYSTEM SPINEVISION, INC.
K954555 10/02/1995 VERSA-FX FEMORAL FIXATION SYSTEM ZIMMER, INC.
K013301 10/03/2001 UNI-T SPINAL SYSTEM SPINEVISION, INC.
K013312 10/04/2001 P.L.U.S. SYSTEM (PIVOT LINK UNIVERSAL SYSTEM) SPINEVISION, INC.
K033508 11/06/2003 PLUS PIVOT LINK UNIVERSAL SYSTEM SPINEVISION, INC.
K964532 11/12/1996 MULTITAK SS SUTURE SYSTEM BONUTTI RESEARCH
K003523 11/15/2000 DEPUY PINNACLE METAL-ON-METAL ACETABULAR CUP LINERS DEPUY ORTHOPAEDICS, INC.
K984378 12/07/1998 DEPUY ACROMED MOSS SPINAL SYSTEM DEPUY, INC.
K955780 12/21/1995 RIGIDYNE A EXTERNAL FIXATION SYSTEM ZIMMER, INC.
K964324 10/30/1996 MULTITAK SS SUTURE SYSTEM BONUTTI RESEARCH


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