Va-Lcp

FDA UDI

Class II (US FDA UDI)

by Synthes

Identity

Trade Name: VA-LCP FDA UDI
Generic Name: Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name: 2.7MM VA-LCP LATERAL DISTAL FIBULA PL/9 HOLES/RT-STERILE FDA UDI
Model / Reference: 02.118.410S FDA UDI
Description: 2.7MM VA-LCP LATERAL DISTAL FIBULA PL/9 HOLES/RT-STERILE FDA UDI

Identifiers

Catalog Number: 02118410S FDA UDI
Primary DI / UDI-DI: 10886982038999 FDA UDI
510(k) Number: K120854 FDA UDI
FDA Product Code: HWC FDA UDI
HRS FDA UDI
GMDN Term: Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3040 FDA UDI
888.3030 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic fixation plate, non-bioabsorbable

The VA-LCP (2.7MM VA-LCP Lateral Distal Fibia Plate) is a non-bioabsorbable, sterile orthopedic fixation plate designed for stabilizing fractured bones in the arm, leg, or pelvis, typically used in conjunction with other fixation methods. This device has undergone clinical trials and regulatory approval to ensure its safety and effectiveness.

Similar devices

Also classified as Orthopaedic fixation plate, non-bioabsorbable.

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AXSOS — Stryker Corp. · Class II
Xpert Wrist — NEWCLIP TECHNICS · Class II
ACUMED — ACUMED LLC · Class II
Anatomska ploča medial distal tibia 6 otvora D — Narcissus doo · Class IIb
ORTHOLOC 3DSi CLAW II — WRIGHT MEDICAL TECHNOLOGY, INC. · Class II

Cleared under the same submission

K120854 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: Synthes

Sources (1)

FDA UDI f770f643-70f2-4cbb-85b7-8b629d6fbb7e 36 fields · synced Jul 29, 2026