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NovoGro

Page Type
Cleared 510(K)
510(k) Number
K162087
510(k) Type
Traditional
Applicant
OsteoNovus, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2017
Days to Decision
264 days
Submission Type
Summary

NovoGro

Page Type
Cleared 510(K)
510(k) Number
K162087
510(k) Type
Traditional
Applicant
OsteoNovus, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2017
Days to Decision
264 days
Submission Type
Summary