510(k) K021953
K021953 is an FDA 510(k) premarket notification submitted by Mitek Worldwide for the device "MITEK PDS/PGA STAPLE". The FDA issued a decision of Substantially Equivalent on December 20, 2002. The device falls under product code JDR (Staple, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Mitek Worldwide has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 20, 2002
- Date Received
- June 13, 2002
- 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