FDA 510(k) Application Details - K182848

Device Classification Name Orthopedic Stereotaxic Instrument

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510(K) Number K182848
Device Name Orthopedic Stereotaxic Instrument
Applicant Medtech S.A.
ZAC Eureka - 900 Rue du Mas de Verchant
Montpellier 34000 FR
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Contact Serge Tabet
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Regulation Number 882.4560

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Classification Product Code OLO
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Date Received 10/09/2018
Decision Date 03/22/2019
Decision SESE - SUBST EQUIV
Classification Advisory Committee NE - Neurology
Review Advisory Committee OR - Orthopedic
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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