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DOLPHIX EXTERNAL FIXATION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132363
510(k) Type
Traditional
Applicant
Citieffe S.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2014
Days to Decision
170 days
Submission Type
Statement

DOLPHIX EXTERNAL FIXATION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132363
510(k) Type
Traditional
Applicant
Citieffe S.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2014
Days to Decision
170 days
Submission Type
Statement