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Ulna Shortening Plating System

FDA UDI

Class II (US FDA UDI)

by Skeletal Dynamics L.l.c.

Identity

Trade Name
Ulna Shortening Plating System FDA UDI
Generic Name
Surgical drill guide, reusable FDA UDI
Model / Reference
Oblique Compression Hole Guide FDA UDI

Identifiers

Catalog Number
TPDG-CHG FDA UDI
Primary DI / UDI-DI
00841506116037 FDA UDI
510(k) Number
K201962 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Surgical drill guide, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Category: Surgical drill guide, reusable

Ulna Shortening Plating System by Skeletal Dynamics L.l.c. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical drill guide, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9d2bd5a4-7c7e-440e-81c8-03ca2b703609 35 fields · synced Jun 8, 2026