Last synced on 12 July 2024 at 11:04 pm

KUMAR T-ANCHORS HERNIA SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081366
510(k) Type
Traditional
Applicant
NASHVILLE SURGICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2008
Days to Decision
61 days
Submission Type
Summary

KUMAR T-ANCHORS HERNIA SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081366
510(k) Type
Traditional
Applicant
NASHVILLE SURGICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2008
Days to Decision
61 days
Submission Type
Summary