Product code HWJ— Orthopedic

FDA has cleared 4 devices under product code HWJ between 1987 and 1990, filed by 3 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.

• 19901 clearance
• 19882 clearances
• 19871 clearance

• Buckman Co., Inc.2 clearances
• Danninger Medical Technology, Inc.1 clearance
• Cross Medical Products, Inc.1 clearance

• K895587 — CROSS MEDICAL PRODUCT PEDICLE AWLCross Medical Products, Inc.·1990-01-04
• K875223 — DANNINGER ORTHOPAEDIC AWLDanninger Medical Technology, Inc.·1988-02-17
• K880045 — ACROMED AWL/PUNCH, DEPTH GAUGEBuckman Co., Inc.·1988-02-17
• K870779 — ACROMED WALLIE-HEINIG TROCHARBuckman Co., Inc.·1987-03-09