Identity
- Trade Name
- ActivaScrew™ FDA UDI
- Generic Name
- Bioabsorbable orthopaedic bone screw FDA UDI
- Device Name
- ActivaScrew™ Cannulated 3.5 x 24 mm FDA UDI
- Model / Reference
- B-ASC-3524 FDA UDI
- Description
- ActivaScrew™ Cannulated 3.5 x 24 mm FDA UDI
Identifiers
- Catalog Number
- B-ASC-3524 FDA UDI
- Primary DI / UDI-DI
- E302BASC35249 FDA UDI
- 510(k) Number
- K081392 FDA UDI
- FDA Product Code
- HWC FDA UDI
- GMDN Term
- Bioabsorbable orthopaedic bone screw 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
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 Safe FDA UDI
Dimensions & Sizes
- Size
- Length — 24 Millimeter FDA UDIWidth — 3.5 Millimeter FDA UDI
Category: Bioabsorbable orthopaedic bone screw
ActivaScrew™ by Bioretec Oy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bioabsorbable orthopaedic bone screw.
- MILAGRO — DePuy Mitek, Inc. · Class II
- MILAGRO — Medos International Sàrl · Class II
- 1.5 mm Inion CPS® Baby — Inion , Ltd. · Class II
- Inion Hexalon™ — Inion , Ltd. · Class II
- 2.0 mm Inion CPS® — Inion , Ltd. · Class II
- Arthrex® — Arthrex, Inc. · Class II
- MILAGRO — Medos International Sàrl · Class II
- REUNITE SCREW SYSTEM — Biomet Orthopedics, Inc. · Class II
Cleared under the same submission
K081392 also covers:
- ActivaScrew™ — Bioretec Oy
- ActivaScrew™ — Bioretec Oy
- ActivaScrew™ — Bioretec Oy
- ActivaScrew™ — Bioretec Oy
- ActivaScrew™ — Bioretec Oy
- ActivaScrew™ — Bioretec Oy
- ActivaScrew™ — Bioretec Oy
- ActivaScrew™ — Bioretec Oy
- ActivaScrew™ — Bioretec Oy
- ActivaScrew™ — Bioretec Oy
- ActivaScrew™ — Bioretec Oy
- ActivaScrew™ — Bioretec Oy
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
- Bioretec Oy
Sources (1)
- FDA UDI b9133b33-af81-4a35-a3d7-0ed9d3160932 38 fields · synced Jun 1, 2026