Last synced on 14 November 2025 at 11:06 pm

Foundation Dermal Regeneration Scaffold Plus (DRS+) Duo

Page Type
Cleared 510(K)
510(k) Number
K240298
510(k) Type
Traditional
Applicant
Bionova Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2024
Days to Decision
202 days
Submission Type
Summary

Foundation Dermal Regeneration Scaffold Plus (DRS+) Duo

Page Type
Cleared 510(K)
510(k) Number
K240298
510(k) Type
Traditional
Applicant
Bionova Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2024
Days to Decision
202 days
Submission Type
Summary