Product code KQZ— Orthopedic

FDA has cleared 11 devices under product code KQZ between 1978 and 1988, filed by 10 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.

• 19882 clearances
• 19872 clearances
• 19851 clearance
• 19831 clearance
• 19823 clearances
• 19801 clearance
• 19781 clearance

• Warm & Form, Orthopedic Materials2 clearances
• The Kendal Co.1 clearance
• Tecnol New Jersey Wound Care, Inc.1 clearance
• Technol, Inc.1 clearance
• Physical Diagnostics, Inc.1 clearance
• Howmedica Corp.1 clearance
• Depuy, Inc.1 clearance
• Comfortex, Inc.1 clearance
• Backtrac1 clearance
• Avec Scientific Design Corp.1 clearance

• K884132 — TECNOL BUCKS TRACTION W/HEEL PROTECTORTechnol, Inc.·1988-10-11
• K882640 — TECNOL SECURE-ALL PELVIC TRACTION BELTTecnol New Jersey Wound Care, Inc.·1988-07-27
• K871900 — OVER DRAPE LEG HOLDERAvec Scientific Design Corp.·1987-06-16
• K871296 — T.E.D.(TM) TRACTION DEVICEThe Kendal Co.·1987-04-15
• K854270 — MURPHY ADJUSTABLE SPLINTComfortex, Inc.·1985-12-09
• K831002 — TPG 1000Physical Diagnostics, Inc.·1983-06-24
• K823660 — UNIVERSAL BUCKS TRACTIONWarm & Form, Orthopedic Materials·1982-12-30
• K823163 — UNIVERSAL BUCKS TRACTIONWarm & Form, Orthopedic Materials·1982-11-10
• K821252 — HOFFMAN UNIVERSAL FOOT SUPPORTHowmedica Corp.·1982-06-22
• K802869 — BACKTRAC 90-90 TRACTIONBacktrac·1980-12-11
• K781754 — SPLINT, HOAKE INFLATABLE AIRDepuy, Inc.·1978-11-08