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SYNTHES (USA) HYBRID EXTERNAL FIXATOR MODIFICATIONS

Page Type
Cleared 510(K)
510(k) Number
K073135
510(k) Type
Traditional
Applicant
Synthes (Usa)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2008
Days to Decision
83 days
Submission Type
Summary

SYNTHES (USA) HYBRID EXTERNAL FIXATOR MODIFICATIONS

Page Type
Cleared 510(K)
510(k) Number
K073135
510(k) Type
Traditional
Applicant
Synthes (Usa)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2008
Days to Decision
83 days
Submission Type
Summary