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ORTHOVIEW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032401
510(k) Type
Traditional
Applicant
Omsbar, Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/14/2003
Days to Decision
10 days
Submission Type
Summary

ORTHOVIEW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032401
510(k) Type
Traditional
Applicant
Omsbar, Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/14/2003
Days to Decision
10 days
Submission Type
Summary