Last synced on 25 April 2025 at 11:05 pm

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
K193396
510(k) Type
Traditional
Applicant
Spineart
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
2/5/2020
Days to Decision
61 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
K193396
510(k) Type
Traditional
Applicant
Spineart
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
2/5/2020
Days to Decision
61 days
Submission Type
Summary