FDA 510(k) Applications Submitted by AMY H MOMMAERTS

FDA 510(k) Number Submission Date Device Name Applicant
K000734 03/07/2000 PIONEER SURGICAL TECHNOLOGY EXTENDED GTR, MODEL 501-601 PIONEER SURGICAL TECHNOLOGY
K001709 06/05/2000 TROCHANTERIC REATTACHMENT DEVICE (STANDARD) AND (LONG), MODEL 501-066, 501-067 PIONEER SURGICAL TECHNOLOGY
K002110 07/12/2000 SPL CRIMP SYSTEM PIONEER SURGICAL TECHNOLOGY
K003496 11/13/2000 CANNULATED SCREW SYSTEM PIONEER SURGICAL TECHNOLOGY


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