FDA 510(k) Applications Submitted by DAVID J STUMPO

FDA 510(k) Number Submission Date Device Name Applicant
K190276 02/08/2019 Provident II Hip Stem StelKast, Inc.
K122773 09/10/2012 CROSS-OVER ACETABULAR SHELL & LINER STELKAST COMPANY
K122883 09/20/2012 EXP TIBIAL INSERTS AND PATELLAR COMPONENTS FOR THE PROVEN GEN-FLEX TOTAL KNEE SYSTEM STELKAST COMPANY
K063211 10/23/2006 PROVEN KNEE SYSTEM HIGH FLEXION TIBIAL INSERT STELKAST COMPANY


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