Product code NEH— General, Plastic Surgery

AMS FASCIAL-ANCHORING SYSTEM

Classification name
Anchor, Fascial
Device class
Class 2
Regulation
21 CFR 878.4300
Advisory panel
General, Plastic Surgery
Total cleared
1
First cleared
Most recent

Market context for product code NEH

FDA has cleared 1 device under product code NEH, all in 2001, filed by 1 applicant company. 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 NEH

Recent clearances under product code NEH

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