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PERLA® TL Posterior Thoraco-lumbar Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231069
510(k) Type
Traditional
Applicant
Spineart SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
10/25/2023
Days to Decision
194 days
Submission Type
Summary

PERLA® TL Posterior Thoraco-lumbar Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231069
510(k) Type
Traditional
Applicant
Spineart SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
10/25/2023
Days to Decision
194 days
Submission Type
Summary