Last synced on 14 November 2025 at 11:06 pm

ProLift Expandable Spacer System

Page Type
Cleared 510(K)
510(k) Number
K250373
510(k) Type
Traditional
Applicant
Life Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2025
Days to Decision
58 days
Submission Type
Summary

ProLift Expandable Spacer System

Page Type
Cleared 510(K)
510(k) Number
K250373
510(k) Type
Traditional
Applicant
Life Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2025
Days to Decision
58 days
Submission Type
Summary