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COBALT V RADIOPAQUE VERTEBROPLASTY BONE CEMENT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070015
510(k) Type
Abbreviated
Applicant
Biomet Manufacturing Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/2007
Days to Decision
331 days
Submission Type
Summary

COBALT V RADIOPAQUE VERTEBROPLASTY BONE CEMENT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070015
510(k) Type
Abbreviated
Applicant
Biomet Manufacturing Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/2007
Days to Decision
331 days
Submission Type
Summary