510(k) K110110
K110110 is an FDA 510(k) premarket notification submitted by Atrium Medical Corporation for the device "ATRIUM CENTRILFX MESH". The FDA issued a decision of Substantially Equivalent on February 15, 2011. The device falls under product code FTL (Mesh, Surgical, Polymeric), a Class II device regulated under 21 CFR 878.3300. Atrium Medical Corporation has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 15, 2011
- Date Received
- January 14, 2011
- Clearance Type
- Special
- 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