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510(k) K870084

Device
RD 140 SURGICAL BENDER
Applicant
TERRAY MANUFACTURING, INC.
510(k) number
K870084
Product code
HXW  
Decision
Substantially Equivalent (SESE)
Decision date
1987-01-28
Date received
1987-01-08
Regulation
888.4540
Classification name
Bender
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
RAY DESJARDINS
Address
24 Mcgonigal St. W. Arnprior Ontario K7s 1l8 CA

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code HXW  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K872949ACROMED BONE PLATE BENDERBuckman Co., Inc.1987-10-15
K870668DRIVER-BENDER-EXTRACTOR, BONE PINMilitary Engineering, Inc.1987-03-09

Legacy Summary#

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FDA Review#

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