RAYLOR FUSION FUNNEL— 510(k) K872281

Substantially Equivalent

Cedar Surgical, Inc.

FDA 510(k) clearance K872281 for RAYLOR FUSION FUNNEL, Substantially Equivalent on 1987-11-02. Applicant: Cedar Surgical, Inc.. Device class: 1.

Clearance details

Applicant: Cedar Surgical, Inc.
Product code: Code HXR
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1987-06-16
Decision date: 1987-11-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minnetonka, MN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HXR

More clearances from Cedar Surgical, Inc.

K873692 — RAYLOR(TM) DRILL STOP1987-12-17
K873690 — CEDAR(TM) PELVIC CUSHION1987-10-26
K873691 — CEDAR(TM) RETRACTOR RING1987-09-28
K864425 — RAYLOR(TM) DISSECTING HOOK1986-12-12
K864421 — RAYLOR(TM) PERIOSTEAL ELEVATORS1986-11-26

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