Identity
- Trade Name
- Mariner FDA UDI
- Generic Name
- Bone-screw internal spinal fixation system connector FDA UDI
- Device Name
- Mariner Lateral Connector, 30mm FDA UDI
- Model / Reference
- 41-4130 FDA UDI
- Description
- Mariner Lateral Connector, 30mm FDA UDI
Identifiers
- Catalog Number
- 41-4130 FDA UDI
- Primary DI / UDI-DI
- 10889981146726 FDA UDI
- FDA Product Code
- NKB FDA UDI
- GMDN Term
- Bone-screw internal spinal fixation system connector 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: Bone-screw internal spinal fixation system connector
Mariner by SeaSpine Orthopedics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone-screw internal spinal fixation system connector.
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- Zodiac — ALPHATEC SPINE, INC. · Class II
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- LnK Spinal Fixation System — L&K BIOMED CO. , LTD. · Class II
- SOCORE - Spinal Stabilization System — NovaSpine · Class IIb
- APEX Spine System — SPINECRAFT LLC · Class II
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Cleared under the same submission
K160902 also covers:
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
K173882 also covers:
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
- Mariner — SeaSpine Orthopedics Corporation
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
- SeaSpine Orthopedics Corporation
Sources (1)
- FDA UDI f6c3d8fc-e064-4534-9b2b-492c93e6ce95 37 fields · synced Jun 8, 2026