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510(k) K872949

Device
ACROMED BONE PLATE BENDER
Applicant
BUCKMAN CO., INC.
510(k) number
K872949
Product code
HXW  
Decision
Substantially Equivalent (SESE)
Decision date
1987-10-15
Date received
1987-07-28
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
DAVID W SCHLERF
Address
921 Calle Verde Martinez CA US 94553 94553

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
K870668DRIVER-BENDER-EXTRACTOR, BONE PINMilitary Engineering, Inc.1987-03-09
K870084RD 140 SURGICAL BENDERTerray Manufacturing, Inc.1987-01-28

Legacy Summary#

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FDA Review#

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