510(k) K904436
K904436 is an FDA 510(k) premarket notification submitted by Mitek Surgical Products, Inc. for the device "QUICKANCHOR (TM)". The FDA issued a decision of Substantially Equivalent on December 11, 1990. The device falls under product code GAS (Suture, Nonabsorbable, Synthetic, Polyester), a Class II device regulated under 21 CFR 878.5000. Mitek Surgical Products, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 11, 1990
- Date Received
- September 28, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Suture, Nonabsorbable, Synthetic, Polyester
- Device Class
- Class II
- Regulation Number
- 878.5000
- Review Panel
- SU
- Submission Type