Identity
- Trade Name
- CROSSWAY FDA UDI
- Generic Name
- Manual bone mill FDA UDI
- Device Name
- Harvesting Mill, 6mm FDA UDI
- Model / Reference
- 6177.2100S FDA UDI
- Description
- Harvesting Mill, 6mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00889095998689 FDA UDI
- 510(k) Number
- K190598 FDA UDI
- FDA Product Code
- HRX FDA UDI
- GMDN Term
- Manual bone mill FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.1100 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Manual bone mill
Crossway by Globus Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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 98eb28c5-f5fa-4e26-925a-4f4c5d23cb69 35 fields · synced Jun 8, 2026