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STRYKER KWIC NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K140868
510(k) Type
Traditional
Applicant
ORTHOVITA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/2014
Days to Decision
63 days
Submission Type
Summary

STRYKER KWIC NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K140868
510(k) Type
Traditional
Applicant
ORTHOVITA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/2014
Days to Decision
63 days
Submission Type
Summary