510(k) K180910
K180910 is an FDA 510(k) premarket notification submitted by ETHICON, Inc. for the device "ULTRAPRO Mesh and ULTRAPRO ADVANCED". The FDA issued a decision of Substantially Equivalent on Jul 2, 2018. The device falls under product code FTL (Mesh, Surgical, Polymeric), a Class II device regulated under 21 CFR 878.3300. ETHICON, Inc. has 207 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jul 2, 2018
- Date Received
- Apr 6, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Mesh, Surgical, Polymeric
- Device Class
- Class II
- Regulation Number
- 878.3300
- Review Panel
- SU
- Submission Type
- 510(k)