DISCOGRAPHY KIT— 510(k) K960082

Substantially Equivalent

Spinal Specialties, Inc.

FDA 510(k) clearance K960082 for DISCOGRAPHY KIT, Substantially Equivalent on 1996-03-21. Applicant: Spinal Specialties, Inc.. Device class: 2.

Clearance details

Applicant: Spinal Specialties, Inc.
Product code: Code IZG
Device class: Class 2
Regulation: 21 CFR 892.1730
Advisory panel: Radiology
Date received: 1996-01-11
Decision date: 1996-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IZG

K960146 — G.E. STERILE DISPOSABLE RADIOGRAPHIC CONTRAST TRAY1996-02-27
K913436 — PXI PNEUMATIC COMPRESSION PADDLE1992-11-05
K920393 — MU125M MOBILE X-RAY SYSTEM1992-04-06
K910503 — DISCOGRAPHY KIT1991-10-07
K903808 — AMSIS RDS, RADIOGRAPHIC DISCOGRAPHY KIT1991-01-22

More clearances from Spinal Specialties, Inc.

K960100 — SPINAL SPECIALTIES NERVE BLOCK TRAY1996-04-24
K942863 — EPIDURAL NEEDLE1995-08-11
K943319 — GERTIE MARX EPI-SPINAL TRAY1995-06-30
K944029 — CONTINUOUS EPIDURAL ANESTHESIA TRAY1995-06-30
K950820 — SPINAL SPECIALTIES PENCIL-POINT SPINAL NEEDLE1995-06-30

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