Javelin Tailor's Bunion Fixation System

FDA 510(k) K202657 · Nvision Biomedical Technologies, Inc.

Substantially Equivalent

510(k) numberK202657

Submission

Device name
Javelin Tailor's Bunion Fixation System
Applicant
Nvision Biomedical Technologies, Inc.
San Antonio, TX, US
Received
September 14, 2020
Decision date
December 14, 2020
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HRS – Plate, Fixation, Bone
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3030
Specialty
Orthopedic
Implant
Yes

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More from Bonebridge AG

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K260291Vortex5 Tailor's Bunion Correction SystemHRS · Traditional 03/25/2026SE
K253423ToeJack MIS Bunion SystemHRS · Traditional 11/18/2025SE
K252657Impact PEEK Union Nail SystemHTY · Special 09/19/2025SE
K250646Impact PEEK Union Nail SystemHTY · Traditional 06/11/2025SE
K250613SnapHammer Hammertoe Correction SystemHWC · Special 04/02/2025SE
K242896Caliber Intramedullary Fixation SystemHWC · Traditional 02/05/2025SE
K243231Trigon PEEK HA WedgesPLF · Special 11/08/2024SE
K2402503D Printed PEEK Interbody SystemMAX · Traditional 09/17/2024SE
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Questions and answers

When was Javelin Tailor's Bunion Fixation System cleared by the FDA?

Javelin Tailor's Bunion Fixation System (K202657) received a 510(k) decision of Substantially Equivalent on December 14, 2020, 91 days after the submission was received.

What is the product code of K202657?

The FDA product code is HRS – Plate, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3030.