Identity
- Trade Name
- CENTRALOC TIBIAL FIXATION FDA UDI
- Generic Name
- Bioabsorbable orthopaedic bone screw FDA UDI
- Model / Reference
- 905684 FDA UDI
Identifiers
- Catalog Number
- 905684 FDA UDI
- Primary DI / UDI-DI
- 00880304421158 FDA UDI
- 510(k) Number
- K033233 FDA UDI
- FDA Product Code
- MAI FDA UDIHWC FDA UDI
- GMDN Term
- Bioabsorbable orthopaedic bone screw FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 FDA UDI888.3040 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: Bioabsorbable orthopaedic bone screw
Centraloc Tibial Fixation by Biomet Sports Medicine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bioabsorbable orthopaedic bone screw.
- MILAGRO — DePuy Mitek, Inc. · Class II
- ActivaScrew™ — Bioretec Oy · Class II
- MILAGRO — Medos International Sàrl · Class II
- 1.5 mm Inion CPS® Baby — Inion , Ltd. · Class II
- Inion Hexalon™ — Inion , Ltd. · Class II
- 2.0 mm Inion CPS® — Inion , Ltd. · Class II
- Arthrex® — Arthrex, Inc. · Class II
- MILAGRO — Medos International Sàrl · Class II
Cleared under the same submission
K033233 also covers:
- CENTRALOC TIBIAL FIXATION — Biomet Sports Medicine
- CENTRALOC TIBIAL FIXATION — Biomet Sports Medicine
- CENTRALOC TIBIAL FIXATION — Biomet Sports Medicine
- CENTRALOC TIBIAL FIXATION — Biomet Sports Medicine
- CENTRALOC TIBIAL FIXATION — Biomet Sports Medicine
- CENTRALOC TIBIAL FIXATION — Biomet Sports Medicine
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
- Biomet Sports Medicine
Sources (1)
- FDA UDI 232e9da9-2b57-45dd-914a-99671b2c8da0 36 fields · synced Jun 6, 2026