FDA 510(k), K193135, TSolution One Total Knee Application

FDA 510(k), K193135, TSolution One Total Knee Application

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510(K) Number: K193135
Device Name: TSolution One Total Knee Application
Manufacturer: Think Surgical, Inc.
Device Classification Name: Orthopedic Stereotaxic Instrument
Regulation Number: 882.4560
Classification Product Code: OLO
Date Received: 11/12/2019
Decision Date: 12/11/2019
Regulation Medical Specialty: Neurology

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