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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