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APOLLO(TM) KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925242
510(k) Type
Traditional
Applicant
INTERMEDICS ORTHOPEDICS
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
6/4/1993
Days to Decision
231 days
Submission Type
Summary

APOLLO(TM) KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925242
510(k) Type
Traditional
Applicant
INTERMEDICS ORTHOPEDICS
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
6/4/1993
Days to Decision
231 days
Submission Type
Summary