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SYNTHES(USA) SYNTHES HYBRID EXTERNAL FIXATOR

Page Type
Cleared 510(K)
510(k) Number
K950384
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/1995
Days to Decision
110 days
Submission Type
Summary

SYNTHES(USA) SYNTHES HYBRID EXTERNAL FIXATOR

Page Type
Cleared 510(K)
510(k) Number
K950384
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/1995
Days to Decision
110 days
Submission Type
Summary