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RIDGEMATRIX 20/40 MESH, PERIOMATRIX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842163
510(k) Type
Traditional
Applicant
ORTHOMATRIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1984
Days to Decision
71 days

RIDGEMATRIX 20/40 MESH, PERIOMATRIX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842163
510(k) Type
Traditional
Applicant
ORTHOMATRIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1984
Days to Decision
71 days