Identity
- Trade Name
- FITBONE TAA SYSTEM FDA UDI
- Generic Name
- Long bone distraction intramedullary nail, motorized FDA UDI
- Device Name
- FITBONE INTRAMEDULLARY LENGTHENING NAIL TAA0960-T-220 FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- FITBONE INTRAMEDULLARY LENGTHENING NAIL TAA0960-T-220 FDA UDI
Identifiers
- Catalog Number
- 60001856 FDA UDI
- Primary DI / UDI-DI
- 18053340344876 FDA UDI
- 510(k) Number
- K203399 FDA UDI
- FDA Product Code
- HSB FDA UDI
- GMDN Term
- Long bone distraction intramedullary nail, motorized FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3020 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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 9 Millimeter FDA UDILength — 60 Millimeter FDA UDILength — 220 Millimeter FDA UDI
Category: Long bone distraction intramedullary nail, motorized
Fitbone Taa System by Orthofix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Long bone distraction intramedullary nail, motorized.
- ORTHOFIX — Orthofix, Inc. · Class II
- ORTHOFIX — Orthofix, Inc. · Class II
- ORTHOFIX — Orthofix, Inc. · Class II
- ORTHOFIX — Orthofix, Inc. · Class II
- ORTHOFIX — Orthofix, Inc. · Class II
- ORTHOFIX — Orthofix, Inc. · Class II
- ORTHOFIX — Orthofix, Inc. · Class II
- ORTHOFIX — Orthofix, Inc. · Class II
Cleared under the same submission
K203399 also covers:
- FITBONE TAA SYSTEM — Orthofix, Inc.
- FITBONE TAA SYSTEM — Orthofix, Inc.
- FITBONE TAA SYSTEM — Orthofix, Inc.
- FITBONE TAA SYSTEM — Orthofix, Inc.
- FITBONE TAA SYSTEM — Orthofix, Inc.
- FITBONE TAA SYSTEM — Orthofix, Inc.
- FITBONE TAA SYSTEM — Orthofix, Inc.
- FITBONE TAA SYSTEM — Orthofix, Inc.
- FITBONE TAA SYSTEM — Orthofix, Inc.
- FITBONE TAA SYSTEM — Orthofix, Inc.
- FITBONE TAA SYSTEM — Orthofix, Inc.
- FITBONE TAA SYSTEM — Orthofix, 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
- Orthofix, Inc.
Sources (1)
- FDA UDI 411dfa4d-9a01-4d8a-93b8-c7ad157e77e2 37 fields · synced Jun 6, 2026