510(k) K181817
K181817 is an FDA 510(k) premarket notification submitted by Transaortic Medical, Inc. for the device "transGlideXT Expandable Introducer". The FDA issued a decision of Substantially Equivalent on Mar 26, 2019. The device falls under product code DYB (Introducer, Catheter), a Class II device regulated under 21 CFR 870.1340. Transaortic Medical, Inc. has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 26, 2019
- Date Received
- Jul 9, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Introducer, Catheter
- Device Class
- Class II
- Regulation Number
- 870.1340
- Review Panel
- CV
- Submission Type
- 510(k)