Last synced on 14 November 2025 at 11:06 pm

Perla® Posterior Cervico-Thoracic Fixation System

Page Type
Cleared 510(K)
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)
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