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TIBIAL BASEPLATE AUGMENT MODEL KC-22118, KC-22128, KC-22138, KC-22148, KC-22158

Page Type
Cleared 510(K)
510(k) Number
K094017
510(k) Type
Special
Applicant
OMNI LIFE SCIENCE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2010
Days to Decision
66 days
Submission Type
Summary

TIBIAL BASEPLATE AUGMENT MODEL KC-22118, KC-22128, KC-22138, KC-22148, KC-22158

Page Type
Cleared 510(K)
510(k) Number
K094017
510(k) Type
Special
Applicant
OMNI LIFE SCIENCE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2010
Days to Decision
66 days
Submission Type
Summary