Cancellous Fixation Screw & Washer for Use W/Screw

FDA 510(k) K871037 · Concept, Inc.

Substantially Equivalent

510(k) numberK871037

Submission

Device name
Cancellous Fixation Screw & Washer for Use W/Screw
Applicant
Concept, Inc.
Clearwater, FL, US
Received
March 17, 1987
Decision date
March 25, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HWC – Screw, Fixation, Bone
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3040
Specialty
Orthopedic
Implant
Yes

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K253108VEOFIX Snap Off ScrewHWC · Traditional Steps Ortho06/05/2026SE
K261154CoLink® & CoLag® Non-Sterile ScrewsHWC · Special In2Bones USA, LLC05/30/2026SE
K261241TriMed Compression ScrewsHWC · Special TriMed, Inc.05/14/2026SE
K254215Arthrex Beaming SystemHWC · Traditional Arthrex, Inc.05/08/2026SE

More from Arthrex, Inc.

510(k)DeviceDecision
K912640Concept Endosteal Fixation DeviceHWC · Traditional 05/01/1992SE
K912957Concept MicromillHRX · Traditional 10/04/1991SE
K896648Concept Unicompartmental Knee SystemHSX · Traditional 06/05/1990SN
K894929Staple Fixation SystemJDR · Traditional 08/30/1989SE
K892376Intravision(Tm) Arthroscope System (Add'L Appli.)HRX · Traditional 08/01/1989SE
K891109Panda(R) Needle Catheter Jejunostomy TubeKNT · Traditional 05/08/1989SE
K881954Concept Power SystemHSZ · Traditional 11/09/1988SE
K884255Concept CCT-5200, Thermal Therapy SystemILO · Traditional 11/08/1988SE
K882121C-Flo Suction TubeDXQ · Traditional 06/20/1988SE
K880414Tendon HarvesterHRX · Traditional 03/25/1988SE

Questions and answers

When was Cancellous Fixation Screw & Washer for Use W/Screw cleared by the FDA?

Cancellous Fixation Screw & Washer for Use W/Screw (K871037) received a 510(k) decision of Substantially Equivalent on March 25, 1987, 8 days after the submission was received.

What is the product code of K871037?

The FDA product code is HWC – Screw, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3040.