K870059Substantially Equivalent

Mentor Nipple Reconstruction Device

Name: K870059 Mentor Nipple Reconstruction Device
Creator: Mentor Corp.
Published: 1987-02-24
License: https://open.fda.gov/license/

Mentor, Goleta CA / Traditional, Substantially Equivalent

FDA source

K870059 is the FDA 510(k) clearance record for MENTOR NIPPLE RECONSTRUCTION DEVICE, cleared for Mentor Corp. on 1987-02-24. FDA records list 65 510(k) clearances for Mentor Corp., from 1977-07-11 to 2013-04-11. As of 2026-09-10, FDA records show no recalls naming K870059.

Clearance record

Decision date: 1987-02-24
Received: 1987-01-07 (48 days to decision)
Review panel: Unknown
Applicant: Mentor Corp. 600 Pine Ave., Goleta CA
Third party review: No