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Foundation Dermal Regeneration Scaffold (DRS) Solo

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231937
510(k) Type
Traditional
Applicant
Bionova Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2023
Days to Decision
136 days
Submission Type
Summary

Foundation Dermal Regeneration Scaffold (DRS) Solo

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231937
510(k) Type
Traditional
Applicant
Bionova Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2023
Days to Decision
136 days
Submission Type
Summary