Identity
- Trade Name
- GALAXY FIXATION SYSTEM FDA UDI
- Generic Name
- External orthopaedic fixation system, reusable FDA UDI
- Device Name
- Spare part, not medical device, not for sale. Reported for registration of UDI direct marking. FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- Spare part, not medical device, not for sale. Reported for registration of UDI direct marking. FDA UDI
Identifiers
- Catalog Number
- 930026 FDA UDI
- Primary DI / UDI-DI
- 18053504366218 FDA UDI
- 510(k) Number
- K113770 FDA UDI
- FDA Product Code
- KTT FDA UDI
- GMDN Term
- External orthopaedic fixation system, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Conditional FDA UDI
Category: External orthopaedic fixation system, reusable
Galaxy Fixation System by Orthofix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as External orthopaedic fixation system, reusable.
- HOFFMANN — Stryker Corp. · Class II
- Integra® External Fixation System — Ascension Orthopedics, Inc. · Class II
- TransFx™ — Zimmer, Inc. · Class I
- HOFFMANN — Stryker Corp. · Class II
- SIDEKICK — WRIGHT MEDICAL TECHNOLOGY, INC. · Class II
- TENXOR — Stryker Corp. · Class II
- SIDEKICK — WRIGHT MEDICAL TECHNOLOGY, INC. · Class II
- SIDEKICK — WRIGHT MEDICAL TECHNOLOGY, INC. · Class II
Cleared under the same submission
K113770 also covers:
- GALAXY FIXATION GEMINI — Orthofix, Inc.
- GALAXY FIXATION GEMINI — Orthofix, Inc.
- GALAXY FIXATION GEMINI — Orthofix, Inc.
- GALAXY FIXATION GEMINI — Orthofix, Inc.
- GALAXY FIXATION SYSTEM — Orthofix, Inc.
- GALAXY FIXATION SYSTEM — Orthofix, Inc.
- GALAXY FIXATION SYSTEM — Orthofix, Inc.
- GALAXY FIXATION SYSTEM — Orthofix, Inc.
- GALAXY FIXATION SYSTEM — Orthofix, Inc.
- GALAXY FIXATION SYSTEM — Orthofix, Inc.
- GALAXY FIXATION SYSTEM — Orthofix, Inc.
- GALAXY FIXATION 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Orthofix, Inc.
Sources (1)
- FDA UDI e0956412-6567-4b46-a3b1-ac925504e163 36 fields · synced May 30, 2026