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ARTELON CMC SPACER ARTHRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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