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FDA 510(k), K171334, Indego
FDA 510(k), K171334, Indego
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$149.00 USD
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510(K) Number: K171334
Device Name: Indego
Manufacturer: Parker Hannifin Corporation
Device Classification Name: powered exoskeleton
Regulation Number: 890.3480
Classification Product Code: PHL
Date Received: 05/08/2017
Decision Date: 09/08/2017
Regulation Medical Specialty: Physical Medicine
Device Name: Indego
Manufacturer: Parker Hannifin Corporation
Device Classification Name: powered exoskeleton
Regulation Number: 890.3480
Classification Product Code: PHL
Date Received: 05/08/2017
Decision Date: 09/08/2017
Regulation Medical Specialty: Physical Medicine
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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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