510(k) K931782
K931782 is an FDA 510(k) premarket notification submitted by Mitek Surgical Products, Inc. for the device "MITEK GIII ANCHOR". The FDA issued a decision of SN on July 22, 1994. The device falls under product code JDR (Staple, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Mitek Surgical Products, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- July 22, 1994
- Date Received
- April 9, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Staple, Fixation, Bone
- Device Class
- Class II
- Regulation Number
- 888.3030
- Review Panel
- OR
- Submission Type