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Delta

FDA UDI

Class II (US FDA UDI)

by Stryker Leibinger

Identity

Trade Name
DELTA FDA UDI
Generic Name
Bone tap, single-use FDA UDI
Device Name
S-DRILLING TAP, HEX, FOR 3mm SCREW FDA UDI
Model / Reference
73-92001 FDA UDI
Description
S-DRILLING TAP, HEX, FOR 3mm SCREW FDA UDI

Identifiers

Catalog Number
73-92001 FDA UDI
Primary DI / UDI-DI
07613252497639 FDA UDI
510(k) Number
K113109 FDA UDI
FDA Product Code
DZJ FDA UDI
GMDN Term
Bone tap, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4120 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 65.0 Millimeter FDA UDI

Delta by Stryker Leibinger — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K113109 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Leibinger

Sources (1)

  • FDA UDI bd8e26eb-7419-4550-90cf-4b2baafc8d71 37 fields · synced Jun 8, 2026