Identity
- Trade Name
- DISCOVERY FDA UDI
- Generic Name
- Bone-screw internal spinal fixation system, non-sterile FDA UDI
- Device Name
- DISCOVERY SCREW SYSTEM CANNULATED FACET SCREW 4.0 x 17.5mm FDA UDI
- Model / Reference
- 175703017 FDA UDI
- Description
- DISCOVERY SCREW SYSTEM CANNULATED FACET SCREW 4.0 x 17.5mm FDA UDI
Identifiers
- Catalog Number
- 175703017 FDA UDI
- Primary DI / UDI-DI
- 10705034034546 FDA UDI
- 510(k) Number
- K012773 FDA UDI
- FDA Product Code
- MRW FDA UDI
- GMDN Term
- Bone-screw internal spinal fixation system, non-sterile FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Discovery by Depuy Spine, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 U | Pending data |
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Manufacturer
- Manufacturer
- Depuy Spine, Inc.
Sources (1)
- FDA UDI 0625ba27-5f4b-4564-8723-d84f5e41e4f4 37 fields · synced Jun 1, 2026