Last synced on 14 November 2025 at 11:06 pm

ROMEO 2 PAD POSTERIOR AXIAL DEVICE

Page Type
Cleared 510(K)
510(k) Number
K141508
510(k) Type
Traditional
Applicant
SPINEART
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
8/21/2014
Days to Decision
76 days
Submission Type
Summary

ROMEO 2 PAD POSTERIOR AXIAL DEVICE

Page Type
Cleared 510(K)
510(k) Number
K141508
510(k) Type
Traditional
Applicant
SPINEART
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
8/21/2014
Days to Decision
76 days
Submission Type
Summary