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Calix Lumbar Spinal Implant System

Page Type
Cleared 510(K)
510(k) Number
K170119
510(k) Type
Traditional
Applicant
X-Spine Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2017
Days to Decision
259 days
Submission Type
Summary

Calix Lumbar Spinal Implant System

Page Type
Cleared 510(K)
510(k) Number
K170119
510(k) Type
Traditional
Applicant
X-Spine Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2017
Days to Decision
259 days
Submission Type
Summary