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Perla Posterior Cervico-Thoracic Fixation system

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153386
510(k) Type
Traditional
Applicant
SPINEART
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
1/25/2016
Days to Decision
63 days
Submission Type
Summary

Perla Posterior Cervico-Thoracic Fixation system

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153386
510(k) Type
Traditional
Applicant
SPINEART
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
1/25/2016
Days to Decision
63 days
Submission Type
Summary