Medical device licence · 11838 · Class 3
AGC MOLDED TIBIAL COMPONENT
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed September 14, 1999; ended September 9, 2009. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 11838
- Licence holder
- Biomet Orthopedics, Ata Biomet Sports Medicine, Ata Biomet Biologics, Ata Biomet TraumaWarsaw, IN, United States
- Risk class
- Class III (moderate to high risk)
- Licence type
- Single Device
- First licensed
- September 14, 1999
- Ended
- September 9, 2009
- Devices covered
- 1
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- AGC UNIVERSAL FEMORAL COMPONENT INTERLOK
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.