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P.F.C. CRUCIATE RETAING KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963117
510(k) Type
Traditional
Applicant
Johnson & Johnson Professionals, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1996
Days to Decision
86 days
Submission Type
Summary

P.F.C. CRUCIATE RETAING KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963117
510(k) Type
Traditional
Applicant
Johnson & Johnson Professionals, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1996
Days to Decision
86 days
Submission Type
Summary