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MODIFICATION TO STRYKER PAINPUMP2

Page Type
Cleared 510(K)
510(k) Number
K030885
510(k) Type
Special
Applicant
STRYKER INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2003
Days to Decision
28 days
Submission Type
Summary

MODIFICATION TO STRYKER PAINPUMP2

Page Type
Cleared 510(K)
510(k) Number
K030885
510(k) Type
Special
Applicant
STRYKER INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2003
Days to Decision
28 days
Submission Type
Summary