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MODIFICATION TO STRYKER PAINPUMP

Page Type
Cleared 510(K)
510(k) Number
K031249
510(k) Type
Traditional
Applicant
STRYKER INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2003
Days to Decision
94 days
Submission Type
Summary

MODIFICATION TO STRYKER PAINPUMP

Page Type
Cleared 510(K)
510(k) Number
K031249
510(k) Type
Traditional
Applicant
STRYKER INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2003
Days to Decision
94 days
Submission Type
Summary