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Small Diameter 2n1 Post Cutter

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
Small Diameter 2n1 Post Cutter FDA UDI
Generic Name
Wire cutter FDA UDI
Model / Reference
SSI005360 FDA UDI

Identifiers

Catalog Number
SSI005360 FDA UDI
Primary DI / UDI-DI
00889024581050 FDA UDI
510(k) Number
K060694 FDA UDI
FDA Product Code
KWS FDA UDI
KWT FDA UDI
GMDN Term
Wire cutter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 FDA UDI
888.3650 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: Wire cutter

Small Diameter 2n1 Post Cutter by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wire cutter.

Cleared under the same submission

K060694 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomet Orthopedics, Inc.

Sources (1)

  • FDA UDI ebdd1d52-29c6-48db-9f24-afdf802a9168 36 fields · synced May 29, 2026