Zavation 95-2003

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

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00842166116849 UDI-DI	Date5 Feb 2018Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Zavation
Generic Name: Orthopaedic bone screw (non-sliding)
Model / Reference: 95-2003

Primary DI / UDI-DI: 00842166116849
FDA Product Code: NKG, KWP
GMDN Term: Orthopaedic bone screw (non-sliding)

Device Class: Class II
Regulation Number: 888.3075, 888.3050
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

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Zavation Screw 1010-C-075090-S-C

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Zavation Screw 1010-C-075095-S-C

Class II

See all devices from Zavation →

Properties

Single Use
Implantable
Prescription Use
Lot / Batch Number

Other properties (10)

Sterile: 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