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MODIFIED ANATOMIC MODULAR KNEE (AMK) SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871585
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/21/1987
Days to Decision
89 days

MODIFIED ANATOMIC MODULAR KNEE (AMK) SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871585
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/21/1987
Days to Decision
89 days