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FDA 510(k) Application Details - K002059
Device Classification Name
Appliance, Fixation, Spinal Interlaminal
More FDA Info for this Device
510(K) Number
K002059
Device Name
Appliance, Fixation, Spinal Interlaminal
Applicant
MICRON PRECISION ENGINEERING, INC.
939 EVENING SHADE DR.
SAN PEDRO, CA 90731 US
Other 510(k) Applications for this Company
Contact
FRANK E BAILY
Other 510(k) Applications for this Contact
Regulation Number
888.3050
More FDA Info for this Regulation Number
Classification Product Code
KWP
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
07/06/2000
Decision Date
11/13/2000
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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