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LumiVy™ Lumbar IBF System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223412
510(k) Type
Special
Applicant
Vy Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/2023
Days to Decision
58 days
Submission Type
Summary

LumiVy™ Lumbar IBF System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223412
510(k) Type
Special
Applicant
Vy Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/2023
Days to Decision
58 days
Submission Type
Summary