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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