510(k) K170134
K170134 is an FDA 510(k) premarket notification submitted by Iconlab, Inc. for the device "Reperen Surgical Mesh". The FDA issued a decision of Substantially Equivalent on Aug 9, 2017. The device falls under product code FTL (Mesh, Surgical, Polymeric), a Class II device regulated under 21 CFR 878.3300.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 9, 2017
- Date Received
- Jan 17, 2017
- 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)