Identity
- Trade Name
- PRECICE® STRYDE System FDA UDI
- Generic Name
- Femur intramedullary nail FDA UDI
- Device Name
- Retrograde Femur 10° Bend FDA UDI
- Model / Reference
- PS10.0-80A265 FDA UDI
- Description
- Retrograde Femur 10° Bend FDA UDI
Identifiers
- Catalog Number
- PS10.0-80A265 FDA UDI
- Primary DI / UDI-DI
- 00887517950550 FDA UDI
- 510(k) Number
- K180503 FDA UDI
- FDA Product Code
- HSB FDA UDI
- GMDN Term
- Femur intramedullary nail FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3020 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 10.0 Millimeter FDA UDI
Category: Femur intramedullary nail
PRECICE® STRYDE System by NuVasive Specialized Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Femur intramedullary nail.
- GAMMA — Stryker Corp. · Class II
- A.R.T.™FEMORAL NAIL — Biomet Orthopedics, Inc. · Class II
- T2 ALPHA — Stryker Corp. · Class II
- T2 — Stryker Corp. · Class II
- 130° Ga-mma Nail — Auxein Medical Private Limited · Class II
- ARIX Femur Nail System — Jeil Medical Corporation · Class II
- INTERTAN — Smith & Nephew, Inc. · Class II
- TRIGEN — Smith & Nephew, Inc. · Class II
Cleared under the same submission
K180503 also covers:
- PRECICE® STRYDE System — NuVasive Specialized Orthopedics, Inc.
- PRECICE® STRYDE System — NuVasive Specialized Orthopedics, Inc.
- PRECICE® STRYDE System — NuVasive Specialized Orthopedics, Inc.
- PRECICE® STRYDE System — NuVasive Specialized Orthopedics, Inc.
- PRECICE® STRYDE System — NuVasive Specialized Orthopedics, Inc.
- PRECICE® STRYDE System — NuVasive Specialized Orthopedics, Inc.
- PRECICE® STRYDE System — NuVasive Specialized Orthopedics, Inc.
- PRECICE® STRYDE System — NuVasive Specialized Orthopedics, Inc.
- PRECICE® STRYDE System — NuVasive Specialized Orthopedics, Inc.
- PRECICE® STRYDE System — NuVasive Specialized Orthopedics, Inc.
- PRECICE® STRYDE System — NuVasive Specialized Orthopedics, Inc.
- PRECICE® STRYDE System — NuVasive Specialized Orthopedics, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- NuVasive Specialized Orthopedics, Inc.
Sources (1)
- FDA UDI 4c80ce2b-0eea-4dc5-aa80-13e7fbda3d93 37 fields · synced May 30, 2026