Zavation 13-1045

Zavation 13-1045 is a Class II device made by Zavation, listed in FDA GUDID since 30 Mar 2018 (UDI-DI 00842166176652), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00842166176652 UDI-DI	Date30 Mar 2018Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00842166176652

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Zavation
Generic name: Internal spinal fixation procedure kit, reusable
Model / reference: 13-1045

Primary DI / UDI-DI: 00842166176652
FDA product code: KWP, MNH, MNI
GMDN term: Internal spinal fixation procedure kit, reusable

Device class: Class II
Regulation number: 888.3050, 888.3070
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Prescription use
Lot / batch number

Other properties (12, all answered No)