SPINAL TOUCH— 510(k) K961212

Substantially Equivalent

Fasstech

FDA 510(k) clearance K961212 for SPINAL TOUCH, Substantially Equivalent on 1996-06-12. Applicant: Fasstech. Device class: 1.

Clearance details

Applicant: Fasstech
Product code: Code KQX
Device class: Class 1
Regulation: 21 CFR 888.1500
Advisory panel: Orthopedic
Date received: 1996-03-28
Decision date: 1996-06-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burlington, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KQX

K011827 — ORTELIUS 8002001-08-28
K971079 — INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE1997-07-09
K962377 — 3D-SPINE1996-09-03
K954647 — INCLINOMETER1995-10-30
K943929 — DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)1995-05-15

More clearances from Fasstech

K063447 — INSIGHT DISCOVERY2007-08-16
K033452 — CWAS 10002003-11-28
K023209 — INSIGHT MILLENNIUM III2003-10-10
K011964 — INSIGHT MILLENNIUM PLUS2001-09-20
K011983 — INSIGHT GENESIS2001-08-30

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