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THE LEIBINGER ADVANCE INTERNAL MIDFACE DISTRACTION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092743
510(k) Type
Traditional
Applicant
STRYKER CRANIOMAXILLOFACIAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/2010
Days to Decision
129 days
Submission Type
Summary

THE LEIBINGER ADVANCE INTERNAL MIDFACE DISTRACTION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092743
510(k) Type
Traditional
Applicant
STRYKER CRANIOMAXILLOFACIAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/2010
Days to Decision
129 days
Submission Type
Summary