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TRACER IMPLANTATION KIT, INDEX IMPLANTATION KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110971
510(k) Type
Traditional
Applicant
Navotek Medical, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2012
Days to Decision
279 days
Submission Type
Summary

TRACER IMPLANTATION KIT, INDEX IMPLANTATION KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110971
510(k) Type
Traditional
Applicant
Navotek Medical, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2012
Days to Decision
279 days
Submission Type
Summary