Identity
- Trade Name
- RATTLER FDA UDI
- Generic Name
- Bioabsorbable orthopaedic bone screw FDA UDI
- Model / Reference
- 948064 FDA UDI
Identifiers
- Catalog Number
- 948064 FDA UDI
- Primary DI / UDI-DI
- 00880304443259 FDA UDI
- 510(k) Number
- K041274 FDA UDI
- FDA Product Code
- HWC FDA UDI
- GMDN Term
- Bioabsorbable orthopaedic bone screw FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 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
Rattler by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K041274 also covers:
- Gentle Threads — Biomet Orthopedics, Inc.
- Gentle Threads — Biomet Orthopedics, Inc.
- Gentle Threads — Biomet Orthopedics, Inc.
- Gentle Threads — Biomet Orthopedics, Inc.
- Gentle Threads — Biomet Orthopedics, Inc.
- Gentle Threads — Biomet Orthopedics, Inc.
- Gentle Threads — Biomet Orthopedics, Inc.
- Gentle Threads — Biomet Orthopedics, Inc.
- Gentle Threads — Biomet Orthopedics, Inc.
- Gentle Threads — Biomet Orthopedics, Inc.
- RATTLER — Biomet Orthopedics, Inc.
- RATTLER — 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 8d961714-67cf-4dbd-9475-7bf2344095b5 36 fields · synced Jun 8, 2026