VASOVASOSTOMY STABILIZER PLATFORM DEV— 510(k) K811223

Name: FDA 510(k) clearance K811223
Creator: U.S. Food and Drug Administration
Published: 1981-05-21

Substantially Equivalent

Biomet, Inc.

FDA 510(k) clearance K811223 for VASOVASOSTOMY STABILIZER PLATFORM DEV, Substantially Equivalent on 1981-05-21. Applicant: Biomet, Inc.. Device class: 1.

Clearance details

Applicant: Biomet, Inc.
Product code: Code KOA
Device class: Class 1
Regulation: 21 CFR 876.4730
Advisory panel: Gastroenterology, Urology
Date received: 1981-05-04
Decision date: 1981-05-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KOA

view all

K182664 — FiXcision2018-12-07
K950267 — URETHRAL SUTURE GUIDE1995-01-31
K932465 — LI VASECTOMY1994-03-02
K921546 — VASOVASOSTOMY SET1993-07-02
K931181 — VESITEC SUTURE PASSER1993-05-12

More clearances from Biomet, Inc.

view all

K253434 — OSSTM Orthopedic Salvage System2026-07-01
K251270 — Taperloc® Complete Hip Stem2026-05-19
K241014 — Biomet Kirschner Wires (K-Wires)2024-05-22
K222760 — StageOne Select Hip Cement Spacer Molds2022-12-28
K221968 — StageOne Shoulder Cement Spacer Molds2022-09-15

Data sourced from openFDA. This site is unofficial and independent of the FDA.