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TM ARDIS INTERBODY SYSTEM INSERTER

Page Type
Cleared 510(K)
510(k) Number
K123602
510(k) Type
Traditional
Applicant
ZIMMER TRABECULAR METAL TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2013
Days to Decision
100 days
Submission Type
Summary

TM ARDIS INTERBODY SYSTEM INSERTER

Page Type
Cleared 510(K)
510(k) Number
K123602
510(k) Type
Traditional
Applicant
ZIMMER TRABECULAR METAL TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2013
Days to Decision
100 days
Submission Type
Summary