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FDA 510(k), K182964, ROSA Knee System
FDA 510(k), K182964, ROSA Knee System
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$149.00 USD
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510(K) Number: K182964
Device Name: ROSA Knee System
Manufacturer: Eric DesRosiers
Device Classification Name: Orthopedic Stereotaxic Instrument
Regulation Number: OLO
Classification Product Code: 10/25/2018
Date Received: 01/24/2019
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: ROSA Knee System
Manufacturer: Eric DesRosiers
Device Classification Name: Orthopedic Stereotaxic Instrument
Regulation Number: OLO
Classification Product Code: 10/25/2018
Date Received: 01/24/2019
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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