Identity
- Trade Name
- MAST QUADRANT™ Retractor System FDA UDI
- Generic Name
- Spinal endoscopic-access system FDA UDI
- Device Name
- CAPITAL 9568010 ROT FLEX ARM ATTCHMNT FDA UDI
- Model / Reference
- 9568010 FDA UDI
- Description
- CAPITAL 9568010 ROT FLEX ARM ATTCHMNT FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00885074055121 FDA UDI
- 510(k) Number
- K043602 FDA UDI
- FDA Product Code
- GAD FDA UDIMBH FDA UDI
- GMDN Term
- Spinal endoscopic-access system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI888.3565 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
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: Spinal endoscopic-access system
MAST QUADRANT™ Retractor System by Medtronic Sofamor Danek, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Spinal endoscopic-access system.
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Cleared under the same submission
K043602 also covers:
- MAST QUADRANT™ Retractor System — MEDTRONIC SOFAMOR DANEK, INC.
- MAST QUADRANT™ Retractor System — MEDTRONIC SOFAMOR DANEK, INC.
- MAST QUADRANT™ Retractor System — MEDTRONIC SOFAMOR DANEK, INC.
- MAST QUADRANT™ Retractor System — MEDTRONIC SOFAMOR DANEK, INC.
- MAST QUADRANT™ Retractor System — MEDTRONIC SOFAMOR DANEK, INC.
- MAST QUADRANT™ Retractor System — MEDTRONIC SOFAMOR DANEK, INC.
- MAST QUADRANT™ Retractor System — MEDTRONIC SOFAMOR DANEK, INC.
- MAST QUADRANT™ Retractor System — MEDTRONIC SOFAMOR DANEK, INC.
- MAST QUADRANT™ Retractor System — MEDTRONIC SOFAMOR DANEK, INC.
- MAST QUADRANT™ Retractor System — MEDTRONIC SOFAMOR DANEK, 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 I | Pending data |
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Manufacturer
- Manufacturer
- Medtronic Sofamor Danek, Inc.
Sources (1)
- FDA UDI 70e01fc1-c46f-45ae-9f01-87bb07609507 35 fields · synced Jun 8, 2026