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FDA 510(k) Application Details - K001886
Device Classification Name
Pin, Fixation, Threaded
More FDA Info for this Device
510(K) Number
K001886
Device Name
Pin, Fixation, Threaded
Applicant
HOWMEDICA OSTEONICS CORP.
359 VETERANS BLVD.
RUTHERFORD, NJ 07070-2584 US
Other 510(k) Applications for this Company
Contact
JENNIFER A DAUDELIN
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
06/21/2000
Decision Date
07/12/2000
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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