FDA 510(k) Applications Submitted by NICHOLAS TABRIZI

FDA 510(k) Number Submission Date Device Name Applicant
K150231 02/02/2015 Navigated Disc Prep Instruments and CAPSTONE Trials MEDTRONIC SOFAMOR DANEK USA, INC
K110522 02/23/2011 VERTEX RECONSTRUCTION SYSTEM, VERTEX SELECT RECONSTRUCTION SYSTEM MEDTRONIC SOFAMOR DANEK USA, INC.
K070756 03/20/2007 SMITH AND NEPHEW REFLECTION 3 ACETABULAR SYSTEM SMITH & NEPHEW, INC.
K081111 04/18/2008 LEGION HINGE KNEE SYSTEM SMITH & NEPHEW, INC.
K081351 05/14/2008 MODIFICATION TO JOURNEY UNICONDYLAR FEMORAL IMPLANT SMITH & NEPHEW, INC.
K072852 10/04/2007 SL-PLUS STANDARD AND LATERAL HIP STEMS SMITH & NEPHEW, INC.


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