Product code KTZ— Orthopedic

FDA has cleared 7 devices under product code KTZ between 1976 and 1992, filed by 7 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.

• 19921 clearance
• 19841 clearance
• 19831 clearance
• 19821 clearance
• 19811 clearance
• 19801 clearance
• 19761 clearance

• Warner-Lambert Co.1 clearance
• Twin City Surgical, Inc.1 clearance
• Nk Biotechnical Engineering Co.1 clearance
• Mcgaw Laboratories1 clearance
• Fitness Motivation Institute of America1 clearance
• Dr. Micheal A. Sabia1 clearance
• Caldwell, Justiss & Co., Inc.1 clearance

• K921266 — NK MEDICAL MICROMETER, MODEL MC001Nk Biotechnical Engineering Co.·1992-07-14
• K841687 — SKYNDEX ELECTRONIC BODY FAT CALCULACaldwell, Justiss & Co., Inc.·1984-06-28
• K831898 — SCOLIMETERDr. Micheal A. Sabia·1983-07-19
• K820659 — A CALIPERTwin City Surgical, Inc.·1982-03-19
• K810116 — ISOROBIC SKINFOLD CALIPERFitness Motivation Institute of America·1981-02-04
• K800363 — PARKE-DAVIS TOTAL KNEE PROSTHESISWarner-Lambert Co.·1980-03-10
• K760521 — TAPE MEASUREMcgaw Laboratories·1976-11-12