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DEVICE MODIFICATION TO RADIUS SPINAL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070631
510(k) Type
Special
Applicant
STRYKER SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2007
Days to Decision
128 days
Submission Type
Summary

DEVICE MODIFICATION TO RADIUS SPINAL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070631
510(k) Type
Special
Applicant
STRYKER SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2007
Days to Decision
128 days
Submission Type
Summary