Identity
- Trade Name
- OSS MODULAR TIBIAL TRAY TRIAL FDA UDI
- Generic Name
- Knee tibia prosthesis trial, reusable FDA UDI
- Model / Reference
- 110018673 FDA UDI
Identifiers
- Catalog Number
- 110018673 FDA UDI
- Primary DI / UDI-DI
- 00880304678583 FDA UDI
- 510(k) Number
- K141331 FDA UDI
- FDA Product Code
- LPH FDA UDIJDI FDA UDIKRO FDA UDI
- GMDN Term
- Knee tibia prosthesis trial, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3358 FDA UDI888.3350 FDA UDI888.3510 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Knee tibia prosthesis trial, reusable
Oss Modular Tibial Tray Trial by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Knee tibia prosthesis trial, reusable.
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Cleared under the same submission
K141331 also covers:
- COMPRESS OSS FACE ADAPTOR TRIAL — Biomet Orthopedics, Inc.
- COMPRESS OSS TAPER ADAPTOR TRIAL — Biomet Orthopedics, Inc.
- MODULAR NAIL 0 DEGREE LOCK COLLAR TRIAL — Biomet Orthopedics, Inc.
- Modular Nail Lock Collar Trial — Biomet Orthopedics, Inc.
- OSS BOWED COLLARED STEM TRIAL — Biomet Orthopedics, Inc.
- OSS BOWED STEM TRIAL — Biomet Orthopedics, Inc.
- OSS BOWED STEM TRIAL — Biomet Orthopedics, Inc.
- OSS BOWED STEM TRIAL — Biomet Orthopedics, Inc.
- OSS BOWED STEM TRIAL — Biomet Orthopedics, Inc.
- OSS BOWED STEM TRIAL — Biomet Orthopedics, Inc.
- OSS BOWED STEM TRIAL — Biomet Orthopedics, Inc.
- OSS CONICAL AUGMENT TRIAL — Biomet Orthopedics, 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 |
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Manufacturer
- Manufacturer
- Biomet Orthopedics, Inc.
Sources (1)
- FDA UDI 21700857-ebe3-40ab-9d1f-9450ce4dbcea 36 fields · synced May 30, 2026