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ARx Illiac Spinal Screw System

Page Type
Cleared 510(K)
510(k) Number
K203163
510(k) Type
Traditional
Applicant
Life Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2020
Days to Decision
55 days
Submission Type
Summary

ARx Illiac Spinal Screw System

Page Type
Cleared 510(K)
510(k) Number
K203163
510(k) Type
Traditional
Applicant
Life Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2020
Days to Decision
55 days
Submission Type
Summary