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OSTEOBOOST-BMA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062260
510(k) Type
Traditional
Applicant
ORTHOS LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
10/26/2006
Days to Decision
83 days
Submission Type
Summary

OSTEOBOOST-BMA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062260
510(k) Type
Traditional
Applicant
ORTHOS LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
10/26/2006
Days to Decision
83 days
Submission Type
Summary