Last synced on 14 November 2025 at 11:06 pm

PERLA® TL posterior osteosynthesis system

Page Type
Cleared 510(K)
510(k) Number
K203506
510(k) Type
Traditional
Applicant
SPINEART
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
1/15/2021
Days to Decision
46 days
Submission Type
Summary

PERLA® TL posterior osteosynthesis system

Page Type
Cleared 510(K)
510(k) Number
K203506
510(k) Type
Traditional
Applicant
SPINEART
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
1/15/2021
Days to Decision
46 days
Submission Type
Summary