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ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K130267
510(k) Type
Traditional
Applicant
SPINEART
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
5/31/2013
Days to Decision
116 days
Submission Type
Summary

ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K130267
510(k) Type
Traditional
Applicant
SPINEART
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
5/31/2013
Days to Decision
116 days
Submission Type
Summary