FDA 510(k) Application Details - K171525

Device Classification Name Orthopedic Stereotaxic Instrument

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510(K) Number K171525
Device Name Orthopedic Stereotaxic Instrument
Applicant Intellijoint Surgical Inc.
60 Bathurst Drive
Unit 6
Waterloo N2V 2A9 CA
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Contact Brandon Gingrich
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Regulation Number 882.4560

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Classification Product Code OLO
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Date Received 05/25/2017
Decision Date 10/30/2017
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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