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Perla® Posterior Cervico-Thoracic Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190071
510(k) Type
Special
Applicant
Spineart
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
2/25/2019
Days to Decision
41 days
Submission Type
Summary

Perla® Posterior Cervico-Thoracic Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190071
510(k) Type
Special
Applicant
Spineart
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
2/25/2019
Days to Decision
41 days
Submission Type
Summary