Identity
- Trade Name
- ARBOR FDA UDI
- Generic Name
- External orthopaedic fixation system, single-use FDA UDI
- Device Name
- 30° Clamp Post FDA UDI
- Model / Reference
- 1173.0030 FDA UDI
- Description
- 30° Clamp Post FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00889095524901 FDA UDI
- 510(k) Number
- K172438 FDA UDI
- FDA Product Code
- LXT FDA UDIKTT FDA UDI
- GMDN Term
- External orthopaedic fixation system, single-use 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
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: External orthopaedic fixation system, single-use
Arbor by Globus Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as External orthopaedic fixation system, single-use.
- TRUELOK EVO — Orthofix, Inc. · Class II
- Monkey Rings™ External Fixation System — Paragon 28 · Class II
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- TrueLok — Orthofix, Inc. · Class II
- DRACO — HNM TOTAL RECON LLC · Class II
- PREFIX FIXATOR — Orthofix, Inc. · Class II
- RINGFIX — Stryker Corp. · Class II
- SMART TSF — Smith & Nephew, Inc. · Class II
Cleared under the same submission
K172438 also covers:
- ARBOR — GLOBUS MEDICAL, INC.
- ARBOR — GLOBUS MEDICAL, INC.
- ARBOR — GLOBUS MEDICAL, INC.
- ARBOR — GLOBUS MEDICAL, INC.
- ARBOR — GLOBUS MEDICAL, INC.
- ARBOR — GLOBUS MEDICAL, INC.
- ARBOR — GLOBUS MEDICAL, INC.
- ARBOR — GLOBUS MEDICAL, INC.
- ARBOR — GLOBUS MEDICAL, INC.
- ARBOR — GLOBUS MEDICAL, INC.
- ARBOR — GLOBUS MEDICAL, INC.
- ARBOR — GLOBUS MEDICAL, 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
- Globus Medical, Inc.
Sources (1)
- FDA UDI a7488df2-d582-4707-8f5b-36bd20ae5c17 35 fields · synced Jun 1, 2026