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Imbibe Needle

Page Type
Cleared 510(K)
510(k) Number
K153306
510(k) Type
Special
Applicant
ORTHOVITA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2015
Days to Decision
32 days
Submission Type
Summary

Imbibe Needle

Page Type
Cleared 510(K)
510(k) Number
K153306
510(k) Type
Special
Applicant
ORTHOVITA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2015
Days to Decision
32 days
Submission Type
Summary