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TM ARDIS INTERBODY SYSTEM TM ARDIS INTERBODY SYSTEM INSTRUMENATION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113561
510(k) Type
Traditional
Applicant
Zimmer Trabecular Metal Technology
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/2012
Days to Decision
180 days
Submission Type
Summary

TM ARDIS INTERBODY SYSTEM TM ARDIS INTERBODY SYSTEM INSTRUMENATION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113561
510(k) Type
Traditional
Applicant
Zimmer Trabecular Metal Technology
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/2012
Days to Decision
180 days
Submission Type
Summary