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GRAFTON DBM

Page Type
Cleared 510(K)
510(k) Number
K051188
510(k) Type
Traditional
Applicant
OSTEOTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2006
Days to Decision
238 days
Submission Type
Summary

GRAFTON DBM

Page Type
Cleared 510(K)
510(k) Number
K051188
510(k) Type
Traditional
Applicant
OSTEOTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2006
Days to Decision
238 days
Submission Type
Summary