Last synced on 9 December 2022 at 11:04 pm

LAPAROTOMY BLADDER NECK SUSPENSION KIT WITH BONE ANCHORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971796
510(k) Type
Traditional
Applicant
LOUISVILLE LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1997
Days to Decision
89 days
Submission Type
Summary

LAPAROTOMY BLADDER NECK SUSPENSION KIT WITH BONE ANCHORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971796
510(k) Type
Traditional
Applicant
LOUISVILLE LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1997
Days to Decision
89 days
Submission Type
Summary