Product code HXW— Orthopedic

ACROMED BONE PLATE BENDER

Classification name: Bender
Device class: Class 1
Regulation: 21 CFR 888.4540
Advisory panel: Orthopedic
Total cleared: 3
First cleared: 1987-01-28
Most recent: 1987-10-15

Market context for product code HXW

FDA has cleared 3 devices under product code HXW, all in 1987, 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.

Top applicants under product code HXW

Terray Manufacturing, Inc.1 clearance
Military Engineering, Inc.1 clearance
Buckman Co., Inc.1 clearance

Recent clearances under product code HXW

K872949 — ACROMED BONE PLATE BENDERBuckman Co., Inc.·1987-10-15
K870668 — DRIVER-BENDER-EXTRACTOR, BONE PINMilitary Engineering, Inc.·1987-03-09
K870084 — RD 140 SURGICAL BENDERTerray Manufacturing, Inc.·1987-01-28

Data sourced from openFDA. This site is unofficial and independent of the FDA.