510(k) K261112
- Device
- CastleLoc-P Anterior Cervical Plate System
- Applicant
- L&K BIOMED Co., Ltd.
- 510(k) number
- K261112
- Product code
- KWQ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2026-05-06
- Date received
- 2026-04-03
- Regulation
- 888.3060
- Classification name
- Appliance, Fixation, Spinal Intervertebral Body
- Medical specialty
- Orthopedic
- Review panel
- Orthopedic
- Device class
- 2
- Clearance type
- Special
- Statement or summary
- Summary
- Third party reviewed
- N
- Source
- FDA openFDA 510(k) dataset plus migrated FDA.report data
Related Records
Applicant Contact
- Contact
- Kihyang Kim
- Address
- #101, 201, 202 16-25, Dongbaekjungang-Ro 16 Beon-Gil Giheung-Gu, Yongin-Si KR 17015 17015
FDA Registration Numbers
- 3015709929
- 1450662
- 3004464325
- 3014252644
- 2031917
- 3001239363
- 3023852420
- 1834331
- 3003541440
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- 3015869492
- 3005823819
Source Documents
FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON
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| K250602 | X-PAC® N-GAGE Lumbar Plate System | Expanding Innovations, Inc. | 2025-05-20 |
| K250486 | Skyway Anterior Cervical Plate System | Kyocera Medical Technologies Inc. (KMTI) | 2025-04-10 |
| K243904 | Elegance® Anterior Cervical plate | Clariance | 2025-01-14 |
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