Last synced on 12 July 2024 at 11:04 pm

DEPUY CAS KNEE INSTRUMENTATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043223
510(k) Type
Traditional
Applicant
DEPUY ORTHOPAEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2005
Days to Decision
102 days
Submission Type
Summary

DEPUY CAS KNEE INSTRUMENTATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043223
510(k) Type
Traditional
Applicant
DEPUY ORTHOPAEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2005
Days to Decision
102 days
Submission Type
Summary