Posterior Lateral Plates

by Depuy Orthopaedics, Inc.

510(k) K103408

Posterior Lateral Plates is a Class II device made by Depuy Orthopaedics, Inc., cleared under FDA 510(k) K103408 on 16 Dec 2010, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K103408↗

FDA record

Trust

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Special	NumberK103408	Date16 Dec 2010Cleared	StatusActive

Official records

FDA 510(k) database 510(k) number K103408

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number: K103408
FDA product code: HRS

Device class: Class II
Regulation: 21 CFR Part 888.3030
Advisory committee: Orthopedic
FDA decision: SESE Substantially Equivalent

Other devices from Depuy Orthopaedics, Inc.

S-Rom

Class III
Global Advantage

Class III
Duraloc MARATHON

Class III
Pinnacle Porocoat

Class III

See all devices from Depuy Orthopaedics, Inc. →