510(k) K250334

Device
Fusion Craniofacial Implant; Fusion Skull Implant
Applicant
Kelyniam Global, Inc.
510(k) number
K250334
Product code
GWO
Decision
Substantially Equivalent (SESE)
Decision date
2025-07-25
Date received
2025-02-05
Regulation
882.5320
Classification name
Plate, Cranioplasty, Preformed, Alterable
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Elise Bozzuto
Address
97 River Rd., Suite A Canton CT US 06019 06019

FDA Registration Numbers

Source Documents

510(k) summary PDF

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K182711Customized Craniofacial Implant (CCI), Customized Skull Implant (CSI)Kelyniam Global, Inc.2019-05-21
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K170725Stryker Universal MeshStryker2017-11-13
K170368Sterile NS SystemJeil Medical Corporation2017-09-11
K161821Stryker Universal MeshStryker2016-12-08
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