Last synced on 14 November 2025 at 11:06 pm

THE LEIBINGER ADVANCE INTERNAL MIDFACE DISTRACTION SYSTEM

Page Type
Cleared 510(K)
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)
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