Last synced on 25 April 2025 at 11:05 pm

ProLift Wedge Expandable Spacer System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242826
510(k) Type
Traditional
Applicant
Life Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/2024
Days to Decision
20 days
Submission Type
Summary

ProLift Wedge Expandable Spacer System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242826
510(k) Type
Traditional
Applicant
Life Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/2024
Days to Decision
20 days
Submission Type
Summary