DeviceClearance

Product code NOV— Orthopedic

MITEK MICRO QUICKANCHOR

Classification name
Anchor, Suture, Bone Fixation, Metallic
Device class
Class 2
Regulation
21 CFR 888.3030
Advisory panel
Orthopedic
Total cleared
1
First cleared
Most recent

FDA classification definition

“This device is indicated for attaching suture into bone for suspension of the nasal valve and for attaching suture into bone at the lower orbital rim.”

— U.S. Food and Drug Administration, device classification record for product code NOV under 21 CFR 888.3030, via openFDA

Market context for product code NOV

FDA has cleared 1 device under product code NOV, all in 2003, 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 NOV

Recent clearances under product code NOV

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