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FDA 510(k) Application Details - K182425
Device Classification Name
Plate, Cranioplasty, Preformed, Alterable
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510(K) Number
K182425
Device Name
Plate, Cranioplasty, Preformed, Alterable
Applicant
Stryker Leibinger GmbH & Co. KG
Boetzinger Strasse 41
Freiburg D-79111 DE
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Contact
Gregory Gohl
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Regulation Number
882.5320
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Classification Product Code
GWO
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More FDA Info for this Product Code
Date Received
09/06/2018
Decision Date
11/06/2018
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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