Medical Device Manufacturer · US , Draper , UT

Ortho Development Corp. - FDA 510(k) Cleared Devices

45 submissions · 43 cleared · Since 1996

Recent clearances: Balanced Knee System TriMax Porous Femoral Components, Trivicta® Hip Stem, BKS Revision System

View 45 510(k) Devices ↓

45

Total

43

Cleared

0

Denied

FDA 510(k) Regulatory Record - Ortho Development Corp. Gastroenterology & Urology ✕

1 devices

1-1 of 1

Cleared Dec 09, 1997

ORION MEDICAL INC. DISPOSABLE BRAIN BIOPSY NEEDLE FOR STEROTACTIC GUIDED BIOPSY

Gastroenterology & Urology · 36d