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SULZER ORTHOPEDICS APOLLO REVISION/CONSTRAINED KNEE TIBIAL BASEPLATE STEM PLUGS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983733
510(k) Type
Traditional
Applicant
SULZER ORTHOPEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1998
Days to Decision
57 days
Submission Type
Summary

SULZER ORTHOPEDICS APOLLO REVISION/CONSTRAINED KNEE TIBIAL BASEPLATE STEM PLUGS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983733
510(k) Type
Traditional
Applicant
SULZER ORTHOPEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1998
Days to Decision
57 days
Submission Type
Summary