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Mariner MIS

FDA UDI

Class II (US FDA UDI)

by SeaSpine Orthopedics Corporation

Identity

Trade Name
Mariner MIS FDA UDI
Generic Name
Orthopaedic rod reducer FDA UDI
Device Name
TOWER REDUCER FDA UDI
Model / Reference
MM2-000310 FDA UDI
Description
TOWER REDUCER FDA UDI

Identifiers

Catalog Number
MM2-000310 FDA UDI
Primary DI / UDI-DI
10889981178284 FDA UDI
510(k) Number
K191648 FDA UDI
FDA Product Code
OLO FDA UDI
KWQ FDA UDI
NKB FDA UDI
GMDN Term
Orthopaedic rod reducer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 FDA UDI
888.3060 FDA UDI
888.3070 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic rod reducer

Mariner MIS by SeaSpine Orthopedics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic rod reducer.

Cleared under the same submission

K191648 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SeaSpine Orthopedics Corporation

Sources (1)

  • FDA UDI 2fb0bdc5-ba33-4991-80f3-e7e5183f2a1d 35 fields · synced Jun 8, 2026