Product code HTT— Orthopedic

FDA has cleared 4 devices under product code HTT between 1976 and 1986, filed by 4 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
• 19821 clearance
• 19801 clearance
• 19761 clearance

• The Anspach Effort, Inc.1 clearance
• Micro-Aire Surgical Instruments, Inc.1 clearance
• Hall Surgical, Division of Zimmer, Inc.1 clearance
• Cutter Laboratories, Inc.1 clearance

• K862529 — HALL STERILE BURHall Surgical, Division of Zimmer, Inc.·1986-07-15
• K821695 — MICRO-AIRE REPLAC. DRILL BURS FOR ZIMMERMicro-Aire Surgical Instruments, Inc.·1982-07-20
• K802598 — CARBIDE CUTTING INSTRUMENT/INTRAARTICUThe Anspach Effort, Inc.·1980-11-19
• K760236 — BUR, SURGICAL CARBIDECutter Laboratories, Inc.·1976-07-26