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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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