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ARX-LINK CROSS CONNECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070995
510(k) Type
Special
Applicant
LIFE SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2007
Days to Decision
74 days
Submission Type
Summary

ARX-LINK CROSS CONNECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070995
510(k) Type
Special
Applicant
LIFE SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2007
Days to Decision
74 days
Submission Type
Summary