Product code LZV— Orthopedic

PROSTHETIC CEMENT REMOVER

Classification name
System, Cement Removal Extraction
Device class
Class 2
Regulation
21 CFR 888.4580
Advisory panel
Orthopedic
Total cleared
7
First cleared
Most recent

Market context for product code LZV

FDA has cleared 7 devices under product code LZV between 1989 and 2002, filed by 6 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 LZV

Recent clearances under product code LZV

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