510(k) K172315
K172315 is an FDA 510(k) premarket notification submitted by Straub Medical AG for the device "Straub Endovascular System". The FDA issued a decision of Substantially Equivalent on Apr 12, 2018. The device falls under product code MCW (Catheter, Peripheral, Atherectomy), a Class II device regulated under 21 CFR 870.4875.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 12, 2018
- Date Received
- Aug 1, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Peripheral, Atherectomy
- Device Class
- Class II
- Regulation Number
- 870.4875
- Review Panel
- CV
- Submission Type
- 510(k)