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ARTELON STT SPACER

Page Type
Cleared 510(K)
510(k) Number
K061956
510(k) Type
Traditional
Applicant
ARTIMPLANT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/2007
Days to Decision
331 days
Submission Type
Summary

ARTELON STT SPACER

Page Type
Cleared 510(K)
510(k) Number
K061956
510(k) Type
Traditional
Applicant
ARTIMPLANT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/2007
Days to Decision
331 days
Submission Type
Summary