Cleared Traditional

AUTO SUTURE SPINAL NERVE HOOK

Jul 1994
Decision
30d
Days
Class 1
Risk

About This 510(k) Submission

K942969 is an FDA 510(k) clearance for the AUTO SUTURE SPINAL NERVE HOOK, a Instrument, Surgical, Non-powered (Class I — General Controls, product code HAO), submitted by United States Surgical, A Division of Tyco Healthc (Norwalk, US). The FDA issued a Cleared decision on July 20, 1994, 30 days after receiving the submission on June 20, 1994. This device falls under the Neurology review panel. Regulated under 21 CFR 882.4535.

Submission Details

510(k) Number K942969 FDA.gov
FDA Decision Cleared SESE
Date Received June 20, 1994
Decision Date July 20, 1994
Days to Decision 30 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Summary PDF

Device Classification

Product Code HAO — Instrument, Surgical, Non-powered
Device Class Class I — General Controls
CFR Regulation 21 CFR 882.4535

Similar Devices — HAO Instrument, Surgical, Non-powered

All 33
Matreneu Percutaneous Balloon Compression Kit
K220920 · Shenzhen Shineyard Medical Device Co. , Ltd. · Sep 2022
MULLAN GANGLION MICROCOMPRESSION SET
K940973 · Cook, Inc. · Sep 1995
RIB RESECTOR
K951492 · United States Surgical, A Division of Tyco Healthc · May 1995
AUTO SUTURE PITUITARY SPINAL RONGEUR
K943115 · United States Surgical, A Division of Tyco Healthc · Jul 1994
AUTO SUTURE SPINAL CURETTE
K942967 · United States Surgical, A Division of Tyco Healthc · Jul 1994
AUTO SUTURE SPINAL OSTEOTOME
K942968 · United States Surgical, A Division of Tyco Healthc · Jul 1994