Murphy Adjustable Splint

FDA 510(k) K854270 · Comfortex, Inc.

Substantially Equivalent

510(k) numberK854270

Submission

Device name
Murphy Adjustable Splint
Applicant
Comfortex, Inc.
Winona, MN, US
Received
October 23, 1985
Decision date
December 9, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KQZ – Component, Traction, Non-Invasive
Device class
Class I (low risk)
Regulation
21 CFR 888.5890
Specialty
Orthopedic

Other 510(k)s with product code KQZ

510(k)DeviceApplicantDecision
K884132Tecnol Bucks Traction W/Heel ProtectorKQZ · Traditional Technol, Inc.10/11/1988SE
K882640Tecnol Secure-All Pelvic Traction BeltKQZ · Traditional Tecnol New Jersey Wound Care, Inc.07/27/1988SE
K871900Over Drape Leg HolderKQZ · Traditional Avec Scientific Design Corp.06/16/1987SE
K871296T.E.D.(Tm) Traction DeviceKQZ · Traditional The Kendal Co.04/15/1987SE
K831002TPG 1000KQZ · Traditional Physical Diagnostics, Inc.06/24/1983SE
K823660Universal Bucks TractionKQZ · Traditional Warm & Form, Orthopedic Materials12/30/1982SE
K823163Universal Bucks TractionKQZ · Traditional Warm & Form, Orthopedic Materials11/10/1982SE
K821252Hoffman Universal Foot SupportKQZ · Traditional Howmedica Corp.06/22/1982SE
K802869Backtrac 90-90 TractionKQZ · Traditional Backtrac12/11/1980SE
K781754Splint, Hoake Inflatable AirKQZ · Traditional Depuy, Inc.11/08/1978SE

More from Depuy, Inc.

510(k)DeviceDecision
K860037Suspender Orthopedic Suspension DeviceHST · Traditional 01/21/1986SE
K855179Transfer-Trax (TM) Splint TractionHST · Traditional 01/21/1986SE
K855181Comfortex Wheelchair CushionKNN · Traditional 01/13/1986SE

Questions and answers

When was Murphy Adjustable Splint cleared by the FDA?

Murphy Adjustable Splint (K854270) received a 510(k) decision of Substantially Equivalent on December 9, 1985, 47 days after the submission was received.

What is the product code of K854270?

The FDA product code is KQZ – Component, Traction, Non-Invasive, a Class I (low risk) device regulated under 21 CFR 888.5890.