Excavation 5155507

by NuVasive, LLC

Excavation 5155507 is a Class II device made by NuVasive, LLC, cleared under FDA 510(k) K200719 on 2 Dec 2020 and listed in FDA GUDID since 6 Apr 2022 (UDI-DI 00887517057297), active as of 22 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 22 Oct 2026

Documents

FDA submission, from GUDID

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	Number00887517057297 UDI-DI	Date6 Apr 2022Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK200719	Date2 Dec 2020Decided	StatusActive

Official records

AccessGUDID record UDI-DI 00887517057297
FDA 510(k) database 510(k) number K200719

Across registries

2 registries list this device

FDA 510(k) K200719 decided 2 Dec 2020 Active
FDA GUDID UDI-DI 00887517057297 listed 6 Apr 2022 Listed

Timeline

2 dated events

2 Dec 2020 Cleared FDA 510(k) K200719
6 Apr 2022 Listed FDA GUDID 00887517057297

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Excavation
Generic name: Internal spinal fixation procedure kit, reusable
Model / reference: 5155507

Primary DI / UDI-DI: 00887517057297
510(k) Number: K200719
FDA product code: OLO
GMDN term: Internal spinal fixation procedure kit, reusable

Device class: Class II
Regulation number: 882.4560
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)