Last synced on 22 September 2023 at 11:04 pm

PERIOGLAS PLUS - SETTABLE BONE GRAFT SUBSTITUTE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031073
510(k) Type
Traditional
Applicant
NovaBone Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2003
Days to Decision
215 days
Submission Type
Summary

PERIOGLAS PLUS - SETTABLE BONE GRAFT SUBSTITUTE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031073
510(k) Type
Traditional
Applicant
NovaBone Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2003
Days to Decision
215 days
Submission Type
Summary