Last synced on 14 November 2025 at 11:06 pm

SYNTHES (USA) CRANIOMAXILLOFACIAL DISTRACTION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K060138
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2006
Days to Decision
134 days
Submission Type
Summary

SYNTHES (USA) CRANIOMAXILLOFACIAL DISTRACTION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K060138
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2006
Days to Decision
134 days
Submission Type
Summary