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PERLA® TL Posterior Osteosynthesis System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213470
510(k) Type
Traditional
Applicant
Spineart
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
1/21/2022
Days to Decision
85 days
Submission Type
Summary

PERLA® TL Posterior Osteosynthesis System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213470
510(k) Type
Traditional
Applicant
Spineart
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
1/21/2022
Days to Decision
85 days
Submission Type
Summary