Identity
- Trade Name
- NIDO Pedicle Screw System FDA UDI
- Generic Name
- Spinal bone screw, non-bioabsorbable FDA UDI
- Device Name
- Bone Screw, Fenestrated Cortical, 10.5 x 105mm FDA UDI
- Model / Reference
- 15-BCC-0505 FDA UDI
- Description
- Bone Screw, Fenestrated Cortical, 10.5 x 105mm FDA UDI
Identifiers
- Catalog Number
- 15-BCC-0505 FDA UDI
- Primary DI / UDI-DI
- B07315BCC05050 FDA UDI
- 510(k) Number
- K230974 FDA UDI
- FDA Product Code
- NKB FDA UDI
- GMDN Term
- Spinal bone screw, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3070 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Spinal bone screw, non-bioabsorbable
A comprehensive orthopedic solution for spinal fixation and stabilization, featuring a fenestrated cortical design with a screw head adaptor to stabilize rods. Learn more about its features, regulatory compliance, and how it works.
Similar devices
Also classified as Spinal bone screw, non-bioabsorbable.
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- ASPIRON™ ACPSYSTEM — CG MedTech Co., Ltd. · Class II
- Sterile and Non Sterile Spinal System — Shandong Weigao Orthopaedic Device Company Limited. · Class IIb
- OpenLoc-L Spinal Fixation System — L&K BIOMED CO. , LTD. · Class II
- Sterile and Non Sterile Spinal System — Shandong Weigao Orthopaedic Device Company Limited. · Class IIb
- AccelFix Spinal Fixation System (Sterile) — L&K Biomed · Class IIb
- Proficient™ Posterior Cervical Spine System — Spine Wave, Inc. · Class II
Cleared under the same submission
K230974 also covers:
- NIDO Pedicle Screw System — Kalitec Direct LLC
- NIDO Pedicle Screw System — Kalitec Direct LLC
- NIDO Pedicle Screw System — Kalitec Direct LLC
- NIDO Pedicle Screw System — Kalitec Direct LLC
- NIDO Pedicle Screw System — Kalitec Direct LLC
- NIDO Pedicle Screw System — Kalitec Direct LLC
- NIDO Pedicle Screw System — Kalitec Direct LLC
- NIDO Pedicle Screw System — Kalitec Direct LLC
- NIDO Pedicle Screw System — Kalitec Direct LLC
- NIDO Pedicle Screw System — Kalitec Direct LLC
- NIDO Pedicle Screw System — Kalitec Direct LLC
- NIDO Pedicle Screw System — Kalitec Direct LLC
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Kalitec Direct LLC
Sources (1)
- FDA UDI 35ed76b8-e056-48ee-84a7-6d66a8636a1d 35 fields · synced Jul 10, 2026