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PERLA TL Posterior Osteosynthesis System

Page Type
Cleared 510(K)
510(k) Number
K203222
510(k) Type
Traditional
Applicant
SPINEART
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
12/17/2020
Days to Decision
45 days
Submission Type
Summary

PERLA TL Posterior Osteosynthesis System

Page Type
Cleared 510(K)
510(k) Number
K203222
510(k) Type
Traditional
Applicant
SPINEART
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
12/17/2020
Days to Decision
45 days
Submission Type
Summary