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STRYKER KNIFELIGHT

Page Type
Cleared 510(K)
510(k) Number
K961122
510(k) Type
Traditional
Applicant
STRYKER INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/1996
Days to Decision
154 days
Submission Type
Summary

STRYKER KNIFELIGHT

Page Type
Cleared 510(K)
510(k) Number
K961122
510(k) Type
Traditional
Applicant
STRYKER INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/1996
Days to Decision
154 days
Submission Type
Summary