Aptus A-4856.43

by Medartis Inc.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

in data synced 23 Oct 2026

Documents

FDA submission, from GUDID

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number07630008440138 UDI-DI	Date24 Oct 2015Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK112560	Date15 Dec 2011Decided	StatusActive

Official records

AccessGUDID record UDI-DI 07630008440138
FDA 510(k) database 510(k) number K112560

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Aptus
Generic name: Orthopaedic fixation plate, non-bioabsorbable, non-sterile
Model / Ref / Catalog: A-4856.43

Primary DI / UDI-DI: 07630008440138
510(k) Number: K112560
FDA product code: HRS
GMDN term: Orthopaedic fixation plate, non-bioabsorbable, non-sterile

Device class: Class II
Regulation number: 888.3030
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Single use
Prescription use
Lot / batch number

Other properties (11)

Supplied sterile: No
Implantable: No
Contains latex: No
Over-the-counter: No
Convenience kit: No
Combination product: No
HCT/P: No
Premarket exempt: No
Serial number: No
Expiration date: No
Manufacturing date: No