510(k) K163440

Device
Stealth Staple System
Applicant
FIRST RAY LLC
510(k) number
K163440
Product code
JDR  
Decision
Substantially Equivalent (SESE)
Decision date
2017-02-01
Date received
2016-12-08
Regulation
888.3030
Classification name
Staple, Fixation, Bone
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
ROBERT HOY
Address
124 S. 600 W. Suite 100 Logan UT US 84321 84321

FDA Registration Numbers

Source Documents

510(k) summary PDF

Other 510(k) Records For Product Code JDR  

510(k)DeviceApplicantDecision date
K250712Linkt Compression Staple SystemTrax Surgical2025-05-14
K243888Medline UNITE® REFLEX® Hybrid Nitinol Implant SystemMedline Industries, LP2025-04-11
K243742Arthrex DynaNite Nitinol StaplesArthrex, Inc.2025-01-31
K243658TMC Compression Implant SystemTreace Medical Concepts2024-12-26
K242415TMC Compression Implant SystemTreace Medical Concepts2024-09-06
K240212COGNiTiON™ Staple SystemOrtho Solutions UK , Ltd.2024-02-23
K232990A’TOMIC™ Nitinol Fixation SystemRmr Ortho, LLC2024-01-12
K230724arcad® 2.0 Duo & Quadro osteosynthesis compressive staplesNovastep2023-12-04
K232905Medline UNITE® REFLEX® Nitinol Staple KitMedline Industries, LP2023-10-19
K232324StealthFix Intraosseous Fixation SystemMedartis, Inc.2023-08-30
K232387Treace Medical Concepts (TMC) Compression Implant SystemTreace Medical Concepts2023-08-28
K231493NITINEX Memory Compression StapleVilex, LLC2023-08-11
K231885Medline UNITE® REFLEX® Nitinol Staple SystemMedline Industries, LP2023-08-09
K231458Extremity StapleRestor3D2023-08-03
K230550JAWS Nitinol Staple SystemParagon 28, Inc.2023-05-11

Legacy Summary

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FDA Review

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