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DEPUY AMK TOTAL KNEE SYSTEM DEPUY COORDINATE ULTRA KNEE REVISION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982585
510(k) Type
Traditional
Applicant
DEPUY ORTHOPAEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/5/1998
Days to Decision
73 days

DEPUY AMK TOTAL KNEE SYSTEM DEPUY COORDINATE ULTRA KNEE REVISION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982585
510(k) Type
Traditional
Applicant
DEPUY ORTHOPAEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/5/1998
Days to Decision
73 days