Identity
- Trade Name
- BUCK FDA UDI
- Generic Name
- Polymer orthopaedic cement restrictor, non-bioabsorbable FDA UDI
- Device Name
- 30MM BUCK CEMENT PLUG WITH DISPOSABLE INSERTER FDA UDI
- Model / Reference
- 71279424 FDA UDI
- Description
- 30MM BUCK CEMENT PLUG WITH DISPOSABLE INSERTER FDA UDI
Identifiers
- Catalog Number
- 71279424 FDA UDI
- Primary DI / UDI-DI
- 03596010493620 FDA UDI
- FDA Product Code
- LZN FDA UDI
- GMDN Term
- Polymer orthopaedic cement restrictor, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.3300 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
MR Safe FDA UDI
Category: Polymer orthopaedic cement restrictor, non-bioabsorbable
Buck by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Polymer orthopaedic cement restrictor, non-bioabsorbable.
- Cement Plug — SIGNATURE ORTHOPAEDICS PTY LTD · Class II
- MectaPlug PE II — Medacta International · Class II
- Definition — Howmedica Osteonics Corp. · Class II
- Cement Plug — SIGNATURE ORTHOPAEDICS PTY LTD · Class II
- EXETER — Howmedica Osteonics Corp. · Class II
- Bone Plug — Howmedica Osteonics Corp. · Class II
- Bone Plug — Howmedica Osteonics Corp. · Class II
- Restrictor — Howmedica Osteonics Corp. · Class II
Cleared under the same submission
K211176 also covers:
- Conquest FX — Smith & Nephew, Inc.
- Contour — Smith & Nephew, Inc.
- ECHELON — Smith & Nephew, Inc.
- ECHELON — Smith & Nephew, Inc.
- ECHELON — Smith & Nephew, Inc.
- ECHELON — Smith & Nephew, Inc.
- POLARCUP — Smith & Nephew, Inc.
- POLARCUP — Smith & Nephew, Inc.
- POLARCUP — Smith & Nephew, Inc.
- POLARCUP — Smith & Nephew, Inc.
- POLARCUP — Smith & Nephew, Inc.
- R3 — Smith & Nephew, Inc.
K791125 also covers:
- BUCK — Smith & Nephew, Inc.
- BUCK — Smith & Nephew, Inc.
- BUCK — Smith & Nephew, Inc.
- BUCK — Smith & Nephew, Inc.
- BUCK — Smith & Nephew, Inc.
- BUCK — Smith & Nephew, Inc.
- BUCK — Smith & Nephew, Inc.
- PREP-IM — Smith & Nephew, Inc.
- Spectron — Smith & Nephew, Inc.
- Spectron — Smith & Nephew, Inc.
- Spectron — Smith & Nephew, Inc.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI 245beab4-1089-4cfc-a515-c6a934087ec7 36 fields · synced Jun 8, 2026