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FDA 510(k) Application Details - K102777
Device Classification Name
Pin, Fixation, Threaded
More FDA Info for this Device
510(K) Number
K102777
Device Name
Pin, Fixation, Threaded
Applicant
MERETE MEDICAL GMBH
102 ALT LANKWITZ
BERLIN D-12247 DE
Other 510(k) Applications for this Company
Contact
EMMANUEL ANAPLIOTIS
Other 510(k) Applications for this Contact
Regulation Number
888.3040
More FDA Info for this Regulation Number
Classification Product Code
JDW
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/24/2010
Decision Date
12/20/2010
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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