510(k) K950045

Device
KLS-MARTIN MANDIBULAR FRACTURE/RECONSTRUCTION SYSTEM
Applicant
KARL LEIBINGER GMBH U. CO. KG
510(k) number
K950045
Product code
JEY  
Decision
Substantially Equivalent (SESE)
Decision date
1995-03-23
Date received
1995-01-05
Regulation
872.4760
Classification name
Plate, Bone
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
MARK A HELLER
Address
2550 M St. NW Washington DC US 20037 20037

FDA Registration Numbers

Source Documents

510(k) summary PDF

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Legacy Summary

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FDA Review

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