Identity
- Trade Name
- MD-Max ULIF FDA UDI
- Generic Name
- Neurosurgical retraction system, spinal FDA UDI
- Device Name
- MD-Max™ ULIF Retractor Instrument Kit FDA UDI
- Model / Reference
- 43-8000-CA FDA UDI
- Description
- MD-Max™ ULIF Retractor Instrument Kit FDA UDI
Identifiers
- Catalog Number
- 43-8000-CA FDA UDI
- Primary DI / UDI-DI
- 00840019936927 FDA UDI
- 510(k) Number
- K122931 FDA UDI
- FDA Product Code
- MNI FDA UDIMNH FDA UDI
- GMDN Term
- Neurosurgical retraction system, spinal FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3070 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
No
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: Neurosurgical retraction system, spinal
MD-Max ULIF by Precision Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K122931 also covers:
- MD-Max ULIF — Precision Spine, Inc.
- MD-Max ULIF — Precision Spine, Inc.
- MD-Max ULIF — Precision Spine, Inc.
- MD-Max ULIF — Precision Spine, Inc.
- MD-Max ULIF — Precision Spine, Inc.
- MD-Max ULIF — Precision Spine, Inc.
- MD-Max ULIF — Precision Spine, Inc.
- MD-Max ULIF — Precision Spine, Inc.
- MD-Max ULIF — Precision Spine, Inc.
- MD-Max ULIF — Precision Spine, Inc.
- MD-Max ULIF — Precision Spine, Inc.
- MD-Max ULIF — Precision Spine, 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
- Precision Spine, Inc.
Sources (1)
- FDA UDI e5374b0e-21aa-47fb-a243-43ccc0a8f1ea 35 fields · synced May 29, 2026