PRE-LOADED ULTRAFIX RC
FDA 510(k) clearance K013553 · decided 2001-12-19
Clearance details
- K-number
- K013553
- Device name
- PRE-LOADED ULTRAFIX RC
- Applicant
- Linvatec Corp.
- Decision
- Substantially Equivalent
- Date received
- 2001-10-25
- Decision date
- 2001-12-19
- Days to decision
- 55 days
- Clearance type
- Traditional
- Product code
- MBI
- Device class
- 2
- Regulation number
- 888.3040
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Largo, FL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.