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Va-Lcp

FDA UDI

Class II (US FDA UDI)

by Synthes

Identity

Trade Name
VA-LCP FDA UDI
Generic Name
Orthopaedic implant aiming/guiding block attachment tool FDA UDI
Device Name
GUIDE BLOCK FOR 2.7MM VA-LCP LATERAL DISTAL FIBULA PL/RT FDA UDI
Model / Reference
03.118.106 FDA UDI
Description
GUIDE BLOCK FOR 2.7MM VA-LCP LATERAL DISTAL FIBULA PL/RT FDA UDI

Identifiers

Catalog Number
03118106 FDA UDI
Primary DI / UDI-DI
10886982073655 FDA UDI
510(k) Number
K120854 FDA UDI
FDA Product Code
HWC FDA UDI
HRS FDA UDI
GMDN Term
Orthopaedic implant aiming/guiding block attachment tool 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

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 implant aiming/guiding block attachment tool

Va-Lcp by Synthes — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant aiming/guiding block attachment tool.

Cleared under the same submission

K120854 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Synthes

Sources (1)

  • FDA UDI a87429ee-e5c8-47e2-8b71-812bb8777e65 36 fields · synced May 30, 2026