Mitek Worldwide
Mitek Worldwide appears in FDA public data with 0 recalls, 10 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 31, 2004.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K032717 | BIOCRYL RAPIDE INTERFERENCE SCREW | March 31, 2004 |
| K032167 | BIO-INTRAFIX TIBIAL SCREW AND SHEATH | October 15, 2003 |
| K032078 | MITEK MICRO QUICKANCHOR | August 25, 2003 |
| K030995 | MINILOK QUICKANCHOR PLUS | June 26, 2003 |
| K031519 | CUFFLOK ANCHOR | June 6, 2003 |
| K031406 | EXOJET TISSUE MANAGEMENT SYSTEM | May 30, 2003 |
| K024115 | MICROFIX QUICKANCHOR PLUS | March 13, 2003 |
| K023388 | MITEK RAPIDLOC-PDS MENISCAL REPAIR SYSTEM | December 27, 2002 |
| K021953 | MITEK PDS/PGA STAPLE | December 20, 2002 |
| K021883 | BIOFASTIN RC THREADED SUTURE ANCHOR | July 1, 2002 |