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510(k) K781451

Device
FLAT WRENCH
Applicant
ORTHOPEDIC EQUIPMENT CO., INC.
510(k) number
K781451
Product code
HXS  
Decision
Substantially Equivalent (SESE)
Decision date
1978-09-27
Date received
1978-08-23
Regulation
888.4540
Classification name
Twister, Wire
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code HXS  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K833726KLEIN WIRE TIGHTENER/BIONIC WIREBionic Instrument Corp.1983-12-22

Legacy Summary#

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FDA Review#

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