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FDA 510(k) Application Details - K020266
Device Classification Name
Screw, Fixation, Bone
More FDA Info for this Device
510(K) Number
K020266
Device Name
Screw, Fixation, Bone
Applicant
INION LTD.
LAAKARINKATU 2
TAMPERE FIN-33520 FI
Other 510(k) Applications for this Company
Contact
HANNA MARTTILA
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
01/25/2002
Decision Date
02/22/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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