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Juliet® Ti LL Lumbar Interbody Device

Page Type
Cleared 510(K)
510(k) Number
K190877
510(k) Type
Traditional
Applicant
SPINEART
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
5/29/2019
Days to Decision
55 days
Submission Type
Summary

Juliet® Ti LL Lumbar Interbody Device

Page Type
Cleared 510(K)
510(k) Number
K190877
510(k) Type
Traditional
Applicant
SPINEART
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
5/29/2019
Days to Decision
55 days
Submission Type
Summary