Product code FNW— General, Plastic Surgery

MICROMAT W/VARIOUS MODELS

Classification name
Pad, Kelly
Device class
Class 2
Regulation
21 CFR 878.4370
Advisory panel
General, Plastic Surgery
Total cleared
2
First cleared
Most recent

Market context for product code FNW

FDA has cleared 2 devices under product code FNW, all in 1984, filed by 2 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.

Top applicants under product code FNW

Recent clearances under product code FNW

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