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PERIOGLAS-BIOGLASS BONE GRAFT SUBSTITUTE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040278
510(k) Type
Special
Applicant
NovaBone Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2004
Days to Decision
25 days
Submission Type
Summary

PERIOGLAS-BIOGLASS BONE GRAFT SUBSTITUTE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040278
510(k) Type
Special
Applicant
NovaBone Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2004
Days to Decision
25 days
Submission Type
Summary