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FDA 510(k) Application Details - K962011
Device Classification Name
Screw, Fixation, Bone
More FDA Info for this Device
510(K) Number
K962011
Device Name
Screw, Fixation, Bone
Applicant
SYNTHES (USA)
1690 RUSSELL RD.
POST OFFICE BOX 1766
PAOLI, PA 19301 US
Other 510(k) Applications for this Company
Contact
ANGELA J SILVESTRI
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
05/23/1996
Decision Date
08/05/1996
Decision
SN - Substantially Equivalent for Some Indications
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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