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FDA 510(k) Application Details - K072675
Device Classification Name
Arthroscope
More FDA Info for this Device
510(K) Number
K072675
Device Name
Arthroscope
Applicant
SMITH & NEPHEW, INC.
150 Minuteman Road
Andover, MA 01810 US
Other 510(k) Applications for this Company
Contact
JANICE HASELTON
Other 510(k) Applications for this Contact
Regulation Number
888.1100
More FDA Info for this Regulation Number
Classification Product Code
HRX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/21/2007
Decision Date
10/15/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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