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GRAFTCAGE ACX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053080
510(k) Type
Traditional
Applicant
Osteotech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2005
Days to Decision
29 days
Submission Type
Summary

GRAFTCAGE ACX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053080
510(k) Type
Traditional
Applicant
Osteotech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2005
Days to Decision
29 days
Submission Type
Summary