Last synced on 12 October 2025 at 8:21 pm

ORTHOVIEW

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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