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STRYKER KNIFELIGHT, STRYKER ILLUMINATED RETRACTOR

Page Type
Cleared 510(K)
510(k) Number
K981717
510(k) Type
Traditional
Applicant
STRYKER INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1998
Days to Decision
46 days
Submission Type
Summary

STRYKER KNIFELIGHT, STRYKER ILLUMINATED RETRACTOR

Page Type
Cleared 510(K)
510(k) Number
K981717
510(k) Type
Traditional
Applicant
STRYKER INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1998
Days to Decision
46 days
Submission Type
Summary