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HEALIX ADVANCE BR ANCHOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120078
510(k) Type
Traditional
Applicant
DEPUY MITEK INC., JOHNSON AND JOHNSON COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/29/2012
Days to Decision
50 days
Submission Type
Summary

HEALIX ADVANCE BR ANCHOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120078
510(k) Type
Traditional
Applicant
DEPUY MITEK INC., JOHNSON AND JOHNSON COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/29/2012
Days to Decision
50 days
Submission Type
Summary