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KLS-MARTIN MANDIBULAR FRACTURE/RECONSTRUCTION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950045
510(k) Type
Traditional
Applicant
KARL LEIBINGER GMBH U. CO. KG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1995
Days to Decision
77 days
Submission Type
Summary

KLS-MARTIN MANDIBULAR FRACTURE/RECONSTRUCTION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950045
510(k) Type
Traditional
Applicant
KARL LEIBINGER GMBH U. CO. KG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1995
Days to Decision
77 days
Submission Type
Summary