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Small Diameter Cement Plug

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
SMALL DIAMETER CEMENT PLUG FDA UDI
Generic Name
Polymer orthopaedic cement restrictor, non-bioabsorbable FDA UDI
Model / Reference
414996 FDA UDI

Identifiers

Catalog Number
414996 FDA UDI
Primary DI / UDI-DI
00880304370500 FDA UDI
510(k) Number
K020045 FDA UDI
K033280 FDA UDI
FDA Product Code
KWT FDA UDI
JDC FDA UDI
GMDN Term
Polymer orthopaedic cement restrictor, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3650 FDA UDI
888.3150 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Polymer orthopaedic cement restrictor, non-bioabsorbable

Small Diameter Cement Plug by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymer orthopaedic cement restrictor, non-bioabsorbable.

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 03ba7336-c6eb-49d3-9c0e-ec877dee6cf0 36 fields · synced May 31, 2026