ReLine 11455060P

by NuVasive, LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 22 Oct 2026

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	Number00887517035875 UDI-DI	Date25 Feb 2021Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: ReLine
Generic Name: Bone-screw internal spinal fixation system rod
Model / Reference: 11455060P

Primary DI / UDI-DI: 00887517035875
510(k) Number: K180498
FDA Product Code: KWP, NKB, PML
GMDN Term: Bone-screw internal spinal fixation system rod

Device Class: Class II
Regulation Number: 888.3050, 888.3070, 888.3027
GUDID distribution status: In Commercial Distribution

Sterilization Method: Radiation Sterilization

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Properties

Sterile
Single Use
Implantable
Prescription Use
Lot / Batch Number
Expiration Date
Manufacturing Date

Other properties (7)

Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No