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MODIFICATION TO EBI DYNAFIX DIAPHYSEAL CORRECTION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K030372
510(k) Type
Traditional
Applicant
EBI, L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2003
Days to Decision
30 days
Submission Type
Summary

MODIFICATION TO EBI DYNAFIX DIAPHYSEAL CORRECTION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K030372
510(k) Type
Traditional
Applicant
EBI, L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2003
Days to Decision
30 days
Submission Type
Summary