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ProLift Expandable System

Page Type
Cleared 510(K)
510(k) Number
K190488
510(k) Type
Traditional
Applicant
Life Spine Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2019
Days to Decision
145 days
Submission Type
Summary

ProLift Expandable System

Page Type
Cleared 510(K)
510(k) Number
K190488
510(k) Type
Traditional
Applicant
Life Spine Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2019
Days to Decision
145 days
Submission Type
Summary