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PARAMOUNT R IBF DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103228
510(k) Type
Special
Applicant
Theken Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/2011
Days to Decision
64 days
Submission Type
Summary

PARAMOUNT R IBF DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103228
510(k) Type
Special
Applicant
Theken Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/2011
Days to Decision
64 days
Submission Type
Summary