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PERIOGLAS PUTTY-BIOACTIVE BONE GRAFT GEL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063596
510(k) Type
Traditional
Applicant
NovaBone Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2007
Days to Decision
80 days
Submission Type
Summary

PERIOGLAS PUTTY-BIOACTIVE BONE GRAFT GEL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063596
510(k) Type
Traditional
Applicant
NovaBone Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2007
Days to Decision
80 days
Submission Type
Summary