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STYLO Interbody Fusion Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180071
510(k) Type
Traditional
Applicant
Legend Spine Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2018
Days to Decision
114 days
Submission Type
Summary

STYLO Interbody Fusion Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180071
510(k) Type
Traditional
Applicant
Legend Spine Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2018
Days to Decision
114 days
Submission Type
Summary