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ARTELON CMC SPACER ARTHRO

Page Type
Cleared 510(K)
510(k) Number
K061954
510(k) Type
Special
Applicant
ARTIMPLANT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2007
Days to Decision
325 days
Submission Type
Summary

ARTELON CMC SPACER ARTHRO

Page Type
Cleared 510(K)
510(k) Number
K061954
510(k) Type
Special
Applicant
ARTIMPLANT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2007
Days to Decision
325 days
Submission Type
Summary