KIIClass I
Tube, Cement Ventilation
Orthopedic · 21 CFR 888.4230
MDR events1All time
Recalls0All time
Registered firms1Currently listed
510(k) clearances0All time
Recent MDR events
1 adverse event reports on file
Event type breakdown
Other1
Most-reported manufacturers
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
1 firms currently registered for this product code
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for this product code.