Identity
- Trade Name
- AUTO PILOT FDA UDI
- Generic Name
- Craniofacial fixation plate, non-bioabsorbable, non-customized FDA UDI
- Device Name
- BONE SCREWS, CROSS-PIN, AUTO-PILOT FDA UDI
- Model / Reference
- 52-91765 FDA UDI
- Description
- BONE SCREWS, CROSS-PIN, AUTO-PILOT FDA UDI
Identifiers
- Catalog Number
- 52-91765 FDA UDI
- Primary DI / UDI-DI
- 37613327283595 FDA UDI
- 510(k) Number
- K970912 FDA UDI
- FDA Product Code
- HWC FDA UDI
- GMDN Term
- Craniofacial fixation plate, non-bioabsorbable, non-customized FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Dimensions & Sizes
- Size
- Length — 5.0 Millimeter FDA UDI
Category: Craniofacial fixation plate, non-bioabsorbable, non-customized
Auto Pilot by Stryker Leibinger — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K970912 also covers:
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
- Stryker Leibinger
Sources (1)
- FDA UDI 560618ca-5eb6-4e8c-b613-c3124cbc4540 36 fields · synced Jun 8, 2026