FDA 510(k) Application Details - K240625

Device Classification Name Orthopedic Stereotaxic Instrument

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510(K) Number K240625
Device Name Orthopedic Stereotaxic Instrument
Applicant Providence Medical Technology, Inc.
4234 Hacienda Drive Suite 150
Pleasanton, CA 94588 US
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Contact Edward Liou
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Regulation Number 882.4560

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Classification Product Code OLO
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Date Received 03/06/2024
Decision Date 05/03/2024
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

FDA Source Information for K240625


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