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FDA 510(k) Application Details - K022048
Device Classification Name
Appliance, Fixation, Spinal Interlaminal
More FDA Info for this Device
510(K) Number
K022048
Device Name
Appliance, Fixation, Spinal Interlaminal
Applicant
INTERPORE CROSS INTL.
181 TECHNOLOGY DR.
IRVINE, CA 92618-2402 US
Other 510(k) Applications for this Company
Contact
LYNN M RODARTI
Other 510(k) Applications for this Contact
Regulation Number
888.3050
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Classification Product Code
KWP
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More FDA Info for this Product Code
Date Received
06/24/2002
Decision Date
12/04/2002
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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