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FDA 510(k) Applications Submitted by MICHAEL COLLINS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990094
01/12/1999
KMI WRIST FUSION SYSTEM
KINETIKOS MEDICAL, INC.
K991873
06/02/1999
KMI WRIST FUSION SYSTEM
KINETIKOS MEDICAL, INC.
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