Cure LP 900-909-13

by Meditech Spine, LLC

Cure LP 900-909-13 is a Class II device made by Meditech Spine, LLC, cleared under FDA 510(k) K171538 on 16 Jun 2017 and listed in FDA GUDID since 3 Nov 2022 (UDI-DI B167900909130), active as of 23 Oct 2026.

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

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

FDA submission, from GUDID

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberB167900909130 UDI-DI	Date3 Nov 2022Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK171538	Date16 Jun 2017Decided	StatusActive

Official records

FDA 510(k) database 510(k) number K171538

Across registries

2 registries list this device

FDA 510(k) K171538 decided 16 Jun 2017 Active
FDA GUDID UDI-DI B167900909130 listed 3 Nov 2022 Listed

Timeline

2 dated events

16 Jun 2017 Cleared FDA 510(k) K171538
3 Nov 2022 Listed FDA GUDID B167900909130

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Cure LP
Generic name: Instrument tray, reusable
Model / reference: 900-909-13

Primary DI / UDI-DI: B167900909130
510(k) Number: K171538
FDA product code: KWQ
GMDN term: Instrument tray, reusable

Device class: Class II
Regulation number: 888.3060
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
Serial number

Other properties (11, all answered No)