Identity
- Trade Name
- StabiLink®MIS Spinal Fixation System FDA UDI
- Generic Name
- Bone file/rasp, manual, reusable FDA UDI
- Device Name
- Contouring Rasp, 8-6mm FDA UDI
- Model / Reference
- CR-485 FDA UDI
- Description
- Contouring Rasp, 8-6mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00815351021617 FDA UDI
- 510(k) Number
- K123093 FDA UDI
- FDA Product Code
- KWP FDA UDI
- GMDN Term
- Bone file/rasp, manual, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3050 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
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: Bone file/rasp, manual, reusable
StabiLink®MIS Spinal Fixation System by Southern Spine LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K123093 also covers:
- StabiLink®MIS Spinal Fixation System — Southern Spine LLC
- StabiLink®MIS Spinal Fixation System — Southern Spine LLC
- StabiLink®MIS Spinal Fixation System — Southern Spine LLC
- StabiLink®MIS Spinal Fixation System — Southern Spine LLC
- StabiLink®MIS Spinal Fixation System — Southern Spine LLC
- StabiLink®MIS Spinal Fixation System — Southern Spine LLC
- StabiLink®MIS Spinal Fixation System — Southern Spine LLC
- StabiLink®MIS Spinal Fixation System — Southern Spine LLC
- StabiLink®MIS Spinal Fixation System — Southern Spine LLC
- StabiLink®MIS Spinal Fixation System — Southern Spine LLC
- StabiLink®MIS Spinal Fixation System — Southern Spine LLC
- StabiLink®MIS Spinal Fixation System — Southern Spine 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Southern Spine LLC
Sources (1)
- FDA UDI e1113aa8-afe1-4974-91ea-c83eecbc7b5c 35 fields · synced May 31, 2026