Last synced on 20 December 2024 at 11:05 pm

CODMAN DURAL GRAFT IMPLANT, MODELS 80-1471, 80-1472, 80-1473, 80-1474, 80-1475, 80-1476, 80-1477, 80-1478, 80-1480, 80-1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033395
510(k) Type
Traditional
Applicant
Codman & Shurtleff, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2004
Days to Decision
125 days
Submission Type
Summary

CODMAN DURAL GRAFT IMPLANT, MODELS 80-1471, 80-1472, 80-1473, 80-1474, 80-1475, 80-1476, 80-1477, 80-1478, 80-1480, 80-1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033395
510(k) Type
Traditional
Applicant
Codman & Shurtleff, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2004
Days to Decision
125 days
Submission Type
Summary