510(k) K041669
K041669 is an FDA 510(k) premarket notification submitted by Synovis Surgical Innovations for the device "VERITAS DRY COLLAGEN MATRIX, VERITAS DRY OR VERITAS PSD". The FDA issued a decision of Substantially Equivalent on October 27, 2004. The device falls under product code FTM (Mesh, Surgical), a Class II device regulated under 21 CFR 878.3300. Synovis Surgical Innovations has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 27, 2004
- Date Received
- June 21, 2004
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Mesh, Surgical
- Device Class
- Class II
- Regulation Number
- 878.3300
- Review Panel
- SU
- Submission Type