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FDA 510(k), K172315, Straub Endovascular System
FDA 510(k), K172315, Straub Endovascular System
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510(K) Number: K172315
Device Name: Straub Endovascular System
Manufacturer: Straub Medical AG
Device Classification Name: Catheter, Peripheral, Atherectomy
Regulation Number: 870.4875
Classification Product Code: MCW
Date Received: 08/01/2017
Decision Date: 04/12/2018
Regulation Medical Specialty: Cardiovascular
Device Name: Straub Endovascular System
Manufacturer: Straub Medical AG
Device Classification Name: Catheter, Peripheral, Atherectomy
Regulation Number: 870.4875
Classification Product Code: MCW
Date Received: 08/01/2017
Decision Date: 04/12/2018
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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