RAYLOR(TM) PERIOSTEAL ELEVATORS— 510(k) K864421

Name: FDA 510(k) clearance K864421
Creator: U.S. Food and Drug Administration
Published: 1986-11-26

Substantially Equivalent

Cedar Surgical, Inc.

FDA 510(k) clearance K864421 for RAYLOR(TM) PERIOSTEAL ELEVATORS, Substantially Equivalent on 1986-11-26. Applicant: Cedar Surgical, Inc.. Device class: 1.

Clearance details

Applicant: Cedar Surgical, Inc.
Product code: Code GEG
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1986-11-10
Decision date: 1986-11-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minnetonka, MN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GEG

view all

K891894 — ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSE1989-04-12
K891899 — ELEVATORS, VARIOUS TYPES1989-04-12
K890365 — SEPTUM ELEVATOR1989-02-03
K890230 — LIGATURE NEEDLES1989-01-27
K890253 — SURGICAL ELEVATOR1989-01-27

More clearances from Cedar Surgical, Inc.

view all

K873692 — RAYLOR(TM) DRILL STOP1987-12-17
K872281 — RAYLOR FUSION FUNNEL1987-11-02
K873690 — CEDAR(TM) PELVIC CUSHION1987-10-26
K873691 — CEDAR(TM) RETRACTOR RING1987-09-28
K864425 — RAYLOR(TM) DISSECTING HOOK1986-12-12

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