Last synced on 9 May 2025 at 11:05 pm

MODIFICATION TO SURGICAL TITANIUM MESH SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020522
510(k) Type
Special
Applicant
DEPUY ACROMED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2002
Days to Decision
30 days
Submission Type
Summary

MODIFICATION TO SURGICAL TITANIUM MESH SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020522
510(k) Type
Special
Applicant
DEPUY ACROMED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2002
Days to Decision
30 days
Submission Type
Summary