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ANATOMIC MODULAR KNEE (AMK) POSTERIOR STABILIZED

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901406
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/23/1990
Days to Decision
119 days

ANATOMIC MODULAR KNEE (AMK) POSTERIOR STABILIZED

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901406
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/23/1990
Days to Decision
119 days