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BIOMERIX VENTRAL HERNIA REPAIR MESH, MODEL SM3-TAB

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093123
510(k) Type
Traditional
Applicant
BIOMERIX CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2010
Days to Decision
223 days
Submission Type
Summary

BIOMERIX VENTRAL HERNIA REPAIR MESH, MODEL SM3-TAB

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093123
510(k) Type
Traditional
Applicant
BIOMERIX CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2010
Days to Decision
223 days
Submission Type
Summary