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FDA 510(k) Application Details - K060177
Device Classification Name
Plate, Bone
More FDA Info for this Device
510(K) Number
K060177
Device Name
Plate, Bone
Applicant
KLS MARTIN L.P.
11239 ST. JOHNS INDUSTRIAL
PARKWAY SOUTH
JACKSONVILLE, FL 32246 US
Other 510(k) Applications for this Company
Contact
JENNIFER DAMATO
Other 510(k) Applications for this Contact
Regulation Number
872.4760
More FDA Info for this Regulation Number
Classification Product Code
JEY
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/23/2006
Decision Date
04/18/2006
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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