Tyber Medical Pin and Wire System (various)

FDA 510(k) K231339 · Tyber Medical, LLC

Substantially Equivalent

510(k) numberK231339

Submission

Device name
Tyber Medical Pin and Wire System (various)
Applicant
Tyber Medical, LLC
Bethlehem, PA, US
Received
May 8, 2023
Decision date
July 6, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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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K241014Biomet Kirschner Wires (K-Wires)HTY · Traditional Biomet, Inc.05/22/2024SE
K231272OSSIOfiber® Pin Product Family, OSSIOfiber® Compression Screw, OSSIOfiber® Trimmable…HTY · Traditional OSSIO , Ltd.12/01/2023SE
K231147Hammerdesis™ Interphalangeal Fusion SystemHTY · Traditional Intelivation09/14/2023SE
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Questions and answers

When was Tyber Medical Pin and Wire System (various) cleared by the FDA?

Tyber Medical Pin and Wire System (various) (K231339) received a 510(k) decision of Substantially Equivalent on July 6, 2023, 59 days after the submission was received.

What is the product code of K231339?

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