L.M.S. Self-Detachable Broach with Stop

FDA 510(k) K901273 · Med-Tek Corp.

Substantially Equivalent

510(k) numberK901273

Submission

Device name
L.M.S. Self-Detachable Broach with Stop
Applicant
Med-Tek Corp.
Indianapolis, IN, US
Received
March 19, 1990
Decision date
June 5, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HTY – Pin, Fixation, Smooth
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3040
Specialty
Orthopedic
Implant
Yes

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More from OSSIO , Ltd.

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K903234F-19 Total Hip ProsthesisJDI · Traditional 10/10/1990SE
K901687F-24 Femoral Hip ProsthesisLWJ · Traditional 09/07/1990SE
K901451F-20 Cemented Metal-Backed Acetabular CupJDI · Traditional 08/31/1990SN
K900428Anesthesia Breathing CircuitsCAI · Traditional 08/17/1990SE
K901626H.N. Metal Backed Acetabular Cup, NoncementedKWA · Traditional 08/14/1990SE
K901594H.N. Total Hip ProsthesisLWJ · Traditional 08/03/1990SE
K901480F-20 Total Hip ProsthesisJDI · Traditional 06/12/1990SE
K901272Orion Blade Plate for Tibial OsteotomyKTT · Traditional 04/23/1990SE
K901240Astel Non-Metal Backed Acetabular Cup for CementedJDI · Traditional 03/26/1990SE
K894978Bacterial FilterCAH · Traditional 11/02/1989SE

Questions and answers

When was L.M.S. Self-Detachable Broach with Stop cleared by the FDA?

L.M.S. Self-Detachable Broach with Stop (K901273) received a 510(k) decision of Substantially Equivalent on June 5, 1990, 78 days after the submission was received.

What is the product code of K901273?

The FDA product code is HTY – Pin, Fixation, Smooth, a Class II (moderate risk) device regulated under 21 CFR 888.3040.