Hoffmann Dynamic Wrist Fixator

FDA 510(k) K910986 · Howmedica Corp.

Substantially Equivalent

510(k) numberK910986

Submission

Device name
Hoffmann Dynamic Wrist Fixator
Applicant
Howmedica Corp.
Rutherford, NJ, US
Received
March 7, 1991
Decision date
January 16, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KTT – Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3030
Specialty
Orthopedic
Implant
Yes

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Questions and answers

When was Hoffmann Dynamic Wrist Fixator cleared by the FDA?

Hoffmann Dynamic Wrist Fixator (K910986) received a 510(k) decision of Substantially Equivalent on January 16, 1992, 315 days after the submission was received.

What is the product code of K910986?

The FDA product code is KTT – Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, a Class II (moderate risk) device regulated under 21 CFR 888.3030.