Last synced on 14 November 2025 at 11:06 pm

NOVABONE POROUS-BONE GRAFT SCAFFOLD

Page Type
Cleared 510(K)
510(k) Number
K060432
510(k) Type
Traditional
Applicant
NovaBone Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2006
Days to Decision
42 days
Submission Type
Summary

NOVABONE POROUS-BONE GRAFT SCAFFOLD

Page Type
Cleared 510(K)
510(k) Number
K060432
510(k) Type
Traditional
Applicant
NovaBone Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2006
Days to Decision
42 days
Submission Type
Summary