Last synced on 18 April 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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