Product code MNF— General, Plastic Surgery

MEDPOR PTERIONAL SURGICAL IMPLANT

Classification name
Implant, Temporal
Device class
Class 2
Regulation
21 CFR 878.3550
Advisory panel
General, Plastic Surgery
Total cleared
2
First cleared
Most recent

Market context for product code MNF

FDA has cleared 2 devices under product code MNF between 2000 and 2011, 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.

Clearances per year

Top applicants under product code MNF

Recent clearances under product code MNF

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