Last synced on 17 May 2024 at 11:06 pm

MODIFICATION TO: LOCATOR IMPLANT ANCHOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072878
510(k) Type
Special
Applicant
ZEST ANCHORS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2007
Days to Decision
55 days
Submission Type
Statement

MODIFICATION TO: LOCATOR IMPLANT ANCHOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072878
510(k) Type
Special
Applicant
ZEST ANCHORS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2007
Days to Decision
55 days
Submission Type
Statement