Adverse-event reports (MAUDE)
Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.
No adverse-event reports are linked to this device.
Recall history
No recalls linked.
Regulatory clearances
None linked.
Manufacturer compliance record
None in the loaded window.
Similar devices
- 11 X 100mm LAG FASTENER Osteocentric Technologies, Inc.
- 11 X 105mm LAG FASTENER Osteocentric Technologies, Inc.
- 11 X 110mm LAG FASTENER Osteocentric Technologies, Inc.
- 11 X 75mm LAG FASTENER Osteocentric Technologies, Inc.
- 11 X 80mm LAG FASTENER Osteocentric Technologies, Inc.
- 11 X 85mm LAG FASTENER Osteocentric Technologies, Inc.
- 11 X 90mm LAG FASTENER Osteocentric Technologies, Inc.
- 11 X 95mm LAG FASTENER Osteocentric Technologies, Inc.
- 13 X 100mm LAG FASTENER Osteocentric Technologies, Inc.
- 13 X 105mm LAG FASTENER Osteocentric Technologies, Inc.
- 13 X 110mm LAG FASTENER Osteocentric Technologies, Inc.
- 13 X 115mm LAG FASTENER Osteocentric Technologies, Inc.
Select up to two to place side-by-side with this device.