Product code LGG— Orthopedic

27-230 TO 27-234 VARIOUS CAST BREAKERS, WOLF

Classification name: Instrument, Cast Application/Removal, Manual
Device class: Class 1
Regulation: 21 CFR 888.5980
Advisory panel: Orthopedic
Total cleared: 3
First cleared: 1984-01-30
Most recent: 1987-01-28

Market context for product code LGG

FDA has cleared 3 devices under product code LGG between 1984 and 1987, filed by 3 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Clearances per year

19871 clearance
19851 clearance
19841 clearance

Top applicants under product code LGG

Orthopedic Systems, Inc.1 clearance
Buckman Co., Inc.1 clearance
Artiberia1 clearance

Recent clearances under product code LGG

K870100 — PLASTER STANDOrthopedic Systems, Inc.·1987-01-28
K851786 — 27-230 TO 27-234 VARIOUS CAST BREAKERS, WOLFArtiberia·1985-07-09
K834384 — MODULAR EXTREMITY CASTING SUPPORTBuckman Co., Inc.·1984-01-30

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