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Vy Spine™ VyLam™ Laminoplasty System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232471
510(k) Type
Traditional
Applicant
Vy Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/2023
Days to Decision
55 days
Submission Type
Summary

Vy Spine™ VyLam™ Laminoplasty System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232471
510(k) Type
Traditional
Applicant
Vy Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/2023
Days to Decision
55 days
Submission Type
Summary