Product code HTH— Orthopedic

FDA has cleared 3 devices under product code HTH between 1982 and 1986, filed by 2 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.

• 19861 clearance
• 19841 clearance
• 19821 clearance

• Osteotomy Guide Co.2 clearances
• Frontier Products1 clearance

• K861576 — SHORTENING OSTEOTOMY GUIDEOsteotomy Guide Co.·1986-05-12
• K841470 — REESE OSTEOTOMY GUIDE SYSOsteotomy Guide Co.·1984-05-23
• K822305 — ORTHO-LEVELFrontier Products·1982-08-20