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GRAFTON PLUS DBM PASTE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043048
510(k) Type
Traditional
Applicant
Osteotech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2005
Days to Decision
384 days
Submission Type
Summary

GRAFTON PLUS DBM PASTE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043048
510(k) Type
Traditional
Applicant
Osteotech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2005
Days to Decision
384 days
Submission Type
Summary