MITEK MICRO QUICKANCHOR
FDA 510(k) clearance K032078 · decided 2003-08-25
Clearance details
- K-number
- K032078
- Device name
- MITEK MICRO QUICKANCHOR
- Applicant
- Mitek Worldwide
- Decision
- Substantially Equivalent
- Date received
- 2003-07-07
- Decision date
- 2003-08-25
- Days to decision
- 49 days
- Clearance type
- Traditional
- Product code
- NOV
- Device class
- 2
- Regulation number
- 888.3030
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Norwood, MA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.