Last synced on 14 November 2025 at 11:06 pm

Cannulated Screw Internal Fixation System

Page Type
Cleared 510(K)
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)
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