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ProLift Wedge Expandable Spacer System

Page Type
Cleared 510(K)
510(k) Number
K203361
510(k) Type
Traditional
Applicant
Life Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/2021
Days to Decision
121 days
Submission Type
Summary

ProLift Wedge Expandable Spacer System

Page Type
Cleared 510(K)
510(k) Number
K203361
510(k) Type
Traditional
Applicant
Life Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/2021
Days to Decision
121 days
Submission Type
Summary