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GRAFTCAGE ACX

Page Type
Cleared 510(K)
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)
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