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ROMEO® 2 Posterior Osteosynthesis System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172101
510(k) Type
Traditional
Applicant
Spineart
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
9/26/2017
Days to Decision
76 days
Submission Type
Summary

ROMEO® 2 Posterior Osteosynthesis System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172101
510(k) Type
Traditional
Applicant
Spineart
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
9/26/2017
Days to Decision
76 days
Submission Type
Summary