Last synced on 14 November 2025 at 11:06 pm

ZEST IMPLANT ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K925849
510(k) Type
Traditional
Applicant
ZEST ANCHORS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/1994
Days to Decision
730 days
Submission Type
Statement

ZEST IMPLANT ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K925849
510(k) Type
Traditional
Applicant
ZEST ANCHORS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/1994
Days to Decision
730 days
Submission Type
Statement