Medical device licence · 10851 · Class 3
SHERLOCK CORTEX SCREW AND CORTEX SCREW/ANCHOR
No longer licensed: cancelled: quality-system requirement (2003)
Licence status Cancelled: quality-system requirement (2003); first licensed August 27, 1999; ended February 16, 2004. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 10851
- Licence holder
- Doctors Research Group IncSouthbury, CT, United States
- Risk class
- Class III (moderate to high risk)
- Licence type
- Single Device
- First licensed
- August 27, 1999
- Ended
- February 16, 2004
- Devices covered
- 6
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- SHERLOCK TI CORTEX SCREW/SUTURE ANCHOR
- SHERLOCK TI SELF-DRILLING CORTEX SCREW
- SHERLOCK TI SELF-DRILLING CORTEX SCREW/SUTURE ANCHOR
- SHERLOCK TI SELF-TAPPING CORTEX SCREW
- SHERLOCK TI SELF-TAPPING CORTEX SCREW/SUTURE ANCHOR
- T1 MF CORTEX SCREW
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.