510(k) K060520
K060520 is an FDA 510(k) premarket notification submitted by Proxy Biomedical , Ltd. for the device "VITAMESH MACROPOROUS PP SURGICAL MESH". The FDA issued a decision of Substantially Equivalent on March 28, 2006. The device falls under product code FTL (Mesh, Surgical, Polymeric), a Class II device regulated under 21 CFR 878.3300. Proxy Biomedical , Ltd. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 28, 2006
- Date Received
- February 27, 2006
- Clearance Type
- Abbreviated
- 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