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ACCELL CONNEXUS DEMINERALIZED BONE MATRIX PUTTY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060306
510(k) Type
Traditional
Applicant
ISOTIS NV
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2006
Days to Decision
48 days
Submission Type
Summary

ACCELL CONNEXUS DEMINERALIZED BONE MATRIX PUTTY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060306
510(k) Type
Traditional
Applicant
ISOTIS NV
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2006
Days to Decision
48 days
Submission Type
Summary