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Cannulated Screw Internal Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173286
510(k) Type
Traditional
Applicant
Life Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2017
Days to Decision
59 days
Submission Type
Summary

Cannulated Screw Internal Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173286
510(k) Type
Traditional
Applicant
Life Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2017
Days to Decision
59 days
Submission Type
Summary