Delta 70-92040

by Stryker Leibinger

Delta 70-92040 is a Class II device made by Stryker Leibinger, cleared under FDA 510(k) K993061 on 19 Nov 1999 and listed in FDA GUDID since 24 Aug 2016 (UDI-DI 07613252598251), 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	Number07613252598251 UDI-DI	Date24 Aug 2016Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK993061	Date19 Nov 1999Decided	StatusActive

Official records

AccessGUDID record UDI-DI 07613252598251
FDA 510(k) database 510(k) number K993061

Across registries

2 registries list this device

FDA 510(k) K993061 decided 19 Nov 1999 Active
FDA GUDID UDI-DI 07613252598251 listed 24 Aug 2016 Listed

Timeline

2 dated events

19 Nov 1999 Cleared FDA 510(k) K993061
24 Aug 2016 Listed FDA GUDID 07613252598251

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Delta
Generic name: Bone tap, single-use
Model / Ref / Catalog: 70-92040

Primary DI / UDI-DI: 07613252598251
510(k) Number: K993061
FDA product code: DZJ
GMDN term: Bone tap, single-use

Device class: Class II
Regulation number: 872.4120
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

Size: Length — 130.0 Millimeter

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Properties

Sterilise before use
Single use
Prescription use
Lot / batch number

Other properties (11, all answered No)