Brainpro Stryker 6000-024-000

by Pajunk GmbH Medizintechnologie

Brainpro Stryker 6000-024-000 is a Class II device made by Pajunk GmbH Medizintechnologie, cleared under FDA 510(k) K060808 on 25 Jul 2006 and listed in FDA GUDID since 2 Apr 2021 (UDI-DI 04048223099384), 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	Number04048223099384 UDI-DI	Date2 Apr 2021Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK060808	Date25 Jul 2006Decided	StatusActive

Official records

AccessGUDID record UDI-DI 04048223099384
FDA 510(k) database 510(k) number K060808

Across registries

2 registries list this device

FDA 510(k) K060808 decided 25 Jul 2006 Active
FDA GUDID UDI-DI 04048223099384 listed 2 Apr 2021 Listed

Timeline

2 dated events

25 Jul 2006 Cleared FDA 510(k) K060808
2 Apr 2021 Listed FDA GUDID 04048223099384

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Brainpro Stryker
Generic name: Brain biopsy procedure kit
Model / Ref / Catalog: 6000-024-000

Primary DI / UDI-DI: 04048223099384
510(k) Number: K060808
FDA product code: HAW
GMDN term: Brain biopsy procedure kit

Device class: Class II
Regulation number: 882.4560
GUDID distribution status: In Commercial Distribution

Other devices from Pajunk GmbH Medizintechnologie

See all devices from Pajunk GmbH Medizintechnologie →

Properties

Supplied sterile
Single use
Lot / batch number
Expiration date
Manufacturing date

Other properties (10, all answered No)