Identity
- Trade Name
- Mont Blanc Spinal Systems FDA UDI
- Generic Name
- Bone-screw internal spinal fixation system, non-sterile FDA UDI
- Device Name
- ROD Ø:5.5 L:300mm, cobalt chrome FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- ROD Ø:5.5 L:300mm, cobalt chrome FDA UDI
Identifiers
- Catalog Number
- MB1RC55300 FDA UDI
- Primary DI / UDI-DI
- 03663422002273 FDA UDI
- 510(k) Number
- K161387 FDA UDI
- FDA Product Code
- NKB FDA UDIMNI FDA UDIMNH FDA UDIKWP FDA UDIOSH FDA UDI
- GMDN Term
- Bone-screw internal spinal fixation system, non-sterile FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3070 FDA UDI888.3050 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 5.5 Millimeter FDA UDILength — 300 Millimeter FDA UDI
Category: Bone-screw internal spinal fixation system, non-sterile
Mont Blanc Spinal Systems by Spineway SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone-screw internal spinal fixation system, non-sterile.
- TIGER Spine System — CORELINK LLC · Class II
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd. · Class II
- SILVERTON SPINAL FIXATION SYSTEM — BIOMET SPINE LLC · Class II
- POLARIS™ 5.5 SPINAL SYSTEM — BIOMET SPINE LLC · Class II
- Vitality® — BIOMET SPINE LLC · Class II
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd. · Class II
- PASS LP — Medicrea International SA · Class II
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd. · Class II
Cleared under the same submission
K161387 also covers:
- Mont Blanc Evo Systems — Spineway SA
- Mont Blanc Evo Systems — Spineway SA
- Mont Blanc Evo Systems — Spineway SA
- Mont Blanc Evo Systems — Spineway SA
- Mont Blanc Evo Systems — Spineway SA
- Mont Blanc Evo Systems — Spineway SA
- Mont Blanc Evo Systems — Spineway SA
- Mont Blanc Evo Systems — Spineway SA
- Mont Blanc Evo Systems — Spineway SA
- Mont Blanc MIS Spinal Systems — Spineway SA
- Mont Blanc MIS Spinal Systems — Spineway SA
- Mont Blanc MIS Spinal Systems — Spineway SA
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
- Spineway SA
Sources (1)
- FDA UDI d11923e4-024b-44fd-8ff6-c917cddb29bf 37 fields · synced Jun 1, 2026