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Other External Fixation

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
OTHER EXTERNAL FIXATION FDA UDI
Generic Name
Orthopaedic implantable-device cutter FDA UDI
Device Name
HEFTY BITE PIN CUTTER STELLITE JAWS .062 CAP FDA UDI
Model / Reference
210272 FDA UDI
Description
HEFTY BITE PIN CUTTER STELLITE JAWS .062 CAP FDA UDI

Identifiers

Catalog Number
210272 FDA UDI
Primary DI / UDI-DI
03596010102300 FDA UDI
510(k) Number
K093047 FDA UDI
FDA Product Code
KTT FDA UDI
GMDN Term
Orthopaedic implantable-device cutter 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: Orthopaedic implantable-device cutter

Other External Fixation by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implantable-device cutter.

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 7bc93f8e-a282-4fc5-90c8-203e1fe41a1b 36 fields · synced Jun 8, 2026