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SYNTHES (USA) CRANIOMAXILLOFACIAL DISTRACTION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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