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DEVICE MODIFICATION TO RADIUS SPINAL SYSTEM

Page Type
Cleared 510(K)
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)
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