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Medline UNITE® REFLEX® Hybrid Nitinol Implant System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243888
510(k) Type
Traditional
Applicant
Medline Industries, LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2025
Days to Decision
114 days
Submission Type
Summary

Medline UNITE® REFLEX® Hybrid Nitinol Implant System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243888
510(k) Type
Traditional
Applicant
Medline Industries, LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2025
Days to Decision
114 days
Submission Type
Summary