Product code HXO— Orthopedic

FDA has cleared 3 devices under product code HXO between 1977 and 1989, 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.

• 19891 clearance
• 19801 clearance
• 19771 clearance

• Zimmer, Inc.1 clearance
• Depuy, Inc.1 clearance
• Cobot Medical Corp.1 clearance

• K885305 — ACETABULAR CUP PUSHER/IMPACTORCobot Medical Corp.·1989-02-08
• K803165 — ACETABULAR CEMENT COMPRESSORZimmer, Inc.·1980-12-31
• K771072 — INSERTEO, META.-PHAL.&THUMB CARPO-METADepuy, Inc.·1977-06-27