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BIOMERIX SURGICAL MESH, MODEL: RCR-01

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070961
510(k) Type
Traditional
Applicant
BIOMERIX CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2008
Days to Decision
326 days
Submission Type
Summary

BIOMERIX SURGICAL MESH, MODEL: RCR-01

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070961
510(k) Type
Traditional
Applicant
BIOMERIX CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2008
Days to Decision
326 days
Submission Type
Summary