Erisma®-LP

FDA UDI

Class II (US FDA UDI)

by Clariance, Inc.

Identity

Trade Name: Erisma®-LP FDA UDI
Generic Name: Spinal bone screw, non-bioabsorbable FDA UDI
Device Name: MIS CANNULATED POLYAXIAL SCREW FDA UDI
Model / Reference: 13011060 FDA UDI
Description: MIS CANNULATED POLYAXIAL SCREW FDA UDI

Identifiers

Catalog Number: 13011060 FDA UDI
Primary DI / UDI-DI: 03700780615650 FDA UDI
510(k) Number: K162367 FDA UDI
FDA Product Code: MNI FDA UDI
NKB FDA UDI
MNH FDA UDI
GMDN Term: Spinal bone screw, non-bioabsorbable 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

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

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 10.5 Millimeter FDA UDI
Length — 60 Millimeter FDA UDI

Category: Spinal bone screw, non-bioabsorbable

Erisma®-LP by Clariance, 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

K162367 also covers:

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: Clariance, Inc.

Sources (1)

FDA UDI 94ef2219-813f-4253-94de-7c5b5dcb250e 37 fields · synced Jun 8, 2026