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FDA 510(k) Application Details - K002798
Device Classification Name
Plate, Bone
More FDA Info for this Device
510(K) Number
K002798
Device Name
Plate, Bone
Applicant
Codman & Shurtleff, Inc.
325 PARAMOUNT DR.
RAYNHAM, MA 02767-0350 US
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Contact
JAMES M FLAHERTY
Other 510(k) Applications for this Contact
Regulation Number
872.4760
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Classification Product Code
JEY
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/07/2000
Decision Date
12/06/2000
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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