DeviceClearance

Product code FTD— General, Plastic Surgery

ATRICURE DISSECTOR

Classification name
Lamp, Surgical
Device class
Class 2
Regulation
21 CFR 878.4580
Advisory panel
General, Plastic Surgery
Total cleared
29
First cleared
Most recent

Market context for product code FTD

FDA has cleared 29 devices under product code FTD between 1977 and 2013, filed by 24 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code FTD

Adverse events under product code FTD

product code FTD
Malfunction
767
Total
767

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code FTD

Data sourced from openFDA. This site is unofficial and independent of the FDA.