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FDA 510(k) Applications Submitted by TIM MILLER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050969
04/18/2005
INCLOSE SURGICAL MESH SYSTEM
ANULEX TECHNOLOGIES, INC
K061386
05/18/2006
ANCHOR BAND SUTURING SYSTEM, MODEL SR-AB
ANULEX TECHNOLOGIES, INC
K022344
07/19/2002
TRINICA SELECT ANTERIOR CERVICAL PLATE SYSTEM
CENTERPULSE SPINE-TECH, INC.
K033679
11/24/2003
COPSIOS BONE VOID FILLER (BVF)
CENTERPULSE SPINE-TECH, INC.
K062307
08/08/2006
XCLOSE TISSUE REPAIR SYSTEM, MODEL SRS
ANULEX TECHNOLOGIES, INC
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