Identity
- Trade Name
- PEMF - PHYSIO-STIM FDA UDI
- Generic Name
- Metallic spinal interbody fusion cage FDA UDI
- Device Name
- 5302, SHIP ASSY., BONE GROWTH STIMULATOR, PHYSIOSTIM, US FDA UDI
- Model / Reference
- 655302-0001 FDA UDI
- Description
- 5302, SHIP ASSY., BONE GROWTH STIMULATOR, PHYSIOSTIM, US FDA UDI
Identifiers
- Catalog Number
- 5302 FDA UDI
- Primary DI / UDI-DI
- 18257200131969 FDA UDI
- PMA Number
- P850007 FDA UDI
- FDA Product Code
- LOF FDA UDI
- GMDN Term
- Metallic spinal interbody fusion cage FDA UDI
Classification
- Device Class
- Class III 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Metallic spinal interbody fusion cage
Pemf - Physio-Stim by Orthofix US LLC — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Metallic spinal interbody fusion cage.
- KODIAK CERVICAL IMPLANT, 14x16mm, 10mmx6° — MET 1 TECHNOLOGIES, LLC · Class II
- Peridot-PT Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
- CoRoent — Nuvasive, Inc. · Class II
- Kyocera Medical Technologies, Inc. — Kyocera Medical Technologies, Inc. · Class II
- MectaLIF 3D — Medacta International · Class II
- Solar™ Interbody Fusion System — Degen Medical · Class II
- Peridot-TD Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
- ShurFit Lumbar Interbody — Precision Spine, Inc. · Class II
Cleared under the same submission
P850007 also covers:
- Orthofix Osteogenesis Stimulator — Orthofix US LLC
- Orthofix Osteogenesis Stimulator — Orthofix US LLC
- Orthofix Osteogenesis Stimulator — Orthofix US LLC
- Orthofix Osteogenesis Stimulator — Orthofix US LLC
- Orthofix Osteogenesis Stimulator — Orthofix US LLC
- Orthofix Osteogenesis Stimulator — Orthofix US LLC
- Orthofix Osteogenesis Stimulator — Orthofix US LLC
- Orthofix Osteogenesis Stimulator — Orthofix US LLC
- PEMF - PHYSIO-STIM — Orthofix US LLC
- PEMF - PHYSIO-STIM — Orthofix US LLC
- PEMF - PHYSIO-STIM — Orthofix US LLC
- PEMF - PHYSIO-STIM — Orthofix US LLC
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 III | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Orthofix US LLC
Sources (1)
- FDA UDI ad64a3fd-0ad7-4c83-93da-1161a74fbdfe 36 fields · synced Jun 1, 2026