Meridian

FDA UDI

Class II (US FDA UDI)

by SeaSpine Orthopedics Corporation

Identity

Trade Name: Meridian FDA UDI
Generic Name: Spinal bone screw, non-bioabsorbable FDA UDI
Device Name: Fixed Angle Screw, 6.0mm Dia. x 60mm FDA UDI
Model / Reference: RA1-006060 FDA UDI
Description: Fixed Angle Screw, 6.0mm Dia. x 60mm FDA UDI

Identifiers

Catalog Number: RA1-006060 FDA UDI
Primary DI / UDI-DI: 10889981231491 FDA UDI
510(k) Number: K200879 FDA UDI
FDA Product Code: MAX FDA UDI
OVD FDA UDI
GMDN Term: Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3080 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Spinal bone screw, non-bioabsorbable

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

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Also classified as Spinal bone screw, non-bioabsorbable.

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OpenLoc-L Spinal Fixation System — L&K BIOMED CO. , LTD. · Class II
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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

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 7efa72ae-e556-4157-b8da-7baa6e59cee2 36 fields · synced Jun 8, 2026