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APACERAM BONE GRAFT SUBSTITUTE

Page Type
Cleared 510(K)
510(k) Number
K120602
510(k) Type
Special
Applicant
HOYA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2012
Days to Decision
24 days
Submission Type
Summary

APACERAM BONE GRAFT SUBSTITUTE

Page Type
Cleared 510(K)
510(k) Number
K120602
510(k) Type
Special
Applicant
HOYA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2012
Days to Decision
24 days
Submission Type
Summary