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U.S. Department of Health and Human Services

Product Classification

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Device neurological stereotaxic instrument
Regulation Description Stereotaxic instrument.
Regulation Medical Specialty Neurology
Review Panel Neurology
Product CodeHAW
Premarket Review Neurological and Physical Medicine Devices (OHT5)
Neurosurgical, Neurointerventional and Neurodiagnostic Devices (DHT5A)
Submission Type 510(k)
Regulation Number 882.4560
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Summary Malfunction
Reporting
Ineligible
Implanted Device? No
Life-Sustain/Support Device? No
Third Party Review Not Third Party Eligible
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