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FDA 510(k) Application Details - K070389
Device Classification Name
Screw, Fixation, Bone
More FDA Info for this Device
510(K) Number
K070389
Device Name
Screw, Fixation, Bone
Applicant
BIOMET SPORTS MEDICINE, INC.
56 EAST BELL DRIVE
P.O. BOX 587
WARSAW, IN 46581 US
Other 510(k) Applications for this Company
Contact
SUSAN ALEXANDER
Other 510(k) Applications for this Contact
Regulation Number
888.3040
More FDA Info for this Regulation Number
Classification Product Code
HWC
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/09/2007
Decision Date
08/09/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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