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PRO OSTEON 500R

Page Type
Cleared 510(K)
510(k) Number
K063346
510(k) Type
Traditional
Applicant
EBI, L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2007
Days to Decision
166 days
Submission Type
Summary

PRO OSTEON 500R

Page Type
Cleared 510(K)
510(k) Number
K063346
510(k) Type
Traditional
Applicant
EBI, L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2007
Days to Decision
166 days
Submission Type
Summary