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APEX KNEE SYSTEM, MODEL KC-230XY, KC-240XY [ NO HOLES, 2 HOLES]

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080842
510(k) Type
Special
Applicant
Omni Life Science, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2008
Days to Decision
59 days
Submission Type
Summary

APEX KNEE SYSTEM, MODEL KC-230XY, KC-240XY [ NO HOLES, 2 HOLES]

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080842
510(k) Type
Special
Applicant
Omni Life Science, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2008
Days to Decision
59 days
Submission Type
Summary