510(k) K943627
K943627 is an FDA 510(k) premarket notification submitted by Sutures , Ltd. for the device "SURGISILK". The FDA issued a decision of SN on December 5, 1994. The device falls under product code GAP (Suture, Nonabsorbable, Silk), a Class II device regulated under 21 CFR 878.5030. Sutures , Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- December 5, 1994
- Date Received
- July 26, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Suture, Nonabsorbable, Silk
- Device Class
- Class II
- Regulation Number
- 878.5030
- Review Panel
- SU
- Submission Type