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STRYKER UNIVERSAL ACL INSTRUMENTATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K951267
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/1995
Days to Decision
164 days
Submission Type
Summary

STRYKER UNIVERSAL ACL INSTRUMENTATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K951267
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/1995
Days to Decision
164 days
Submission Type
Summary