Identity
- Trade Name
- VERTEX® Reconstruction System FDA UDI
- Generic Name
- Spinal bone screw, non-bioabsorbable FDA UDI
- Device Name
- SCREW 6900606 VAS CANCELLOUS 4.0X6MM TI FDA UDI
- Model / Reference
- 6900606 FDA UDI
- Description
- SCREW 6900606 VAS CANCELLOUS 4.0X6MM TI FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00721902060519 FDA UDI
- 510(k) Number
- K003780 FDA UDI
- FDA Product Code
- KWP FDA UDI
- GMDN Term
- Spinal bone screw, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3050 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
Dimensions & Sizes
- Size
- Length — 6.0 Millimeter FDA UDIOuter Diameter — 4.0 Millimeter FDA UDI
Category: Spinal bone screw, non-bioabsorbable
VERTEX® Reconstruction System by Medtronic Sofamor Danek, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Spinal bone screw, non-bioabsorbable.
- 4CIS® Chiron Spinal Fixation System — ALPHANOX CO., LTD. · Class II
- LnK/PathLoc-L MIS Spinal System — L&K BIOMED CO. , LTD. · Class II
- 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
K003780 also covers:
- CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTEX® Reconstruction System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTEX® Reconstruction System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTEX® Reconstruction System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTEX® Reconstruction System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTEX® Reconstruction System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTEX® Reconstruction System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTEX® Reconstruction System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTEX® Reconstruction System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTEX® Reconstruction System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTEX® Reconstruction System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTEX® Reconstruction System — MEDTRONIC SOFAMOR DANEK, INC.
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
- Medtronic Sofamor Danek, Inc.
Sources (1)
- FDA UDI b11605f5-e9b3-43f2-8bfd-c4f5b43a2329 36 fields · synced Jun 8, 2026