Centerline Cannulated Accessories 6875-065

by Life Spine, 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	Number00190837021139 UDI-DI	Date12 Dec 2017Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK151196	Date14 Jul 2015Decided	StatusActive

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Withdrawn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: Centerline Cannulated Accessories
Generic name: Bone-screw internal spinal fixation system rod
Model / reference: 6875-065

Primary DI / UDI-DI: 00190837021139
510(k) Number: K151196
FDA product code: NKB
GMDN term: Bone-screw internal spinal fixation system rod

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

Sterilisation method: Moist Heat or Steam Sterilization

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Arx 13-5545-13

Class II
Arx 13-5540-13

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Arx 13-6545-13

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See all devices from Life Spine, Inc. →

Properties

Sterilise before use
Single use
Implantable
Prescription use
Lot / batch number

Other properties (10)

Supplied 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