Arthrex®
- Primary DI
- 00888867529823
- Company
- ARTHREX, INC.
- Model
- AR-8974-27K
- Catalog number
- AR-8974-27K
- Device description
- FibuLock® PRO Guidewire, 2.0 x 200mm 2PK
- Published
- 2026-03-16
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- true
Regulatory Flags
- DUNS number
- 131747628
- Device count
- 2
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- true
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
Identifiers
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 10888867529820 | Primary | GS1 | 0 | |
| 00888867529823 | Unit of Use | GS1 | 0 | |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Package type | Contains DI | Discontinue date | Status |
|---|
| 10888867529820 | Primary | GS1 | 0 | | | | |
| 00888867529823 | Unit of Use | GS1 | 0 | | | | |
Product Codes
| Code | Name | Class | Specialty | Regulation | Implant | Malfunction reporting |
|---|
| MDM | Instrument, Manual, Surgical, General Use | 1 | General, Plastic Surgery | 878.4800 | N | Eligible |
Premarket Submissions
No records found.
Premarket Details
No records found.
GMDN Terms
| Term | Definition |
|---|
| Orthopaedic intraoperative positioning pin, single-use | A nonimplantable device in the form of a thin rod intended to be drilled into bone to assist with the positioning of an implantable device and/or surgical instrument (e.g., fixation plate, drill guide) during an orthopaedic procedure. It is also referred to as a wire or temporary K-wire. This is a single-use device. |
Device Sizes
No records found.
Storage And Handling
No records found.
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | Email |
|---|
| +1(800)934-4404 | complaints@arthrex.com |
Other Devices From This Company
Other Devices Sharing Product Codes
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|---|
| 06438394002678 | Activa Instrument | Bioretec Oy | MDM | 2026-03-23 |
| 06438394002685 | Activa Instrument | Bioretec Oy | MDM | 2026-03-23 |
| 06438394002692 | Activa Instrument | Bioretec Oy | MDM | 2026-03-23 |
| 06438394020382 | Activa Instrument | Bioretec Oy | MDM | 2026-03-23 |
| 06438394010956 | Activa Instrument | Bioretec Oy | MDM | 2026-03-23 |
| 00198506089619 | ELMED INCORPORATED | ELMED INCORPORATED | MDM | 2026-03-17 |
| 00888867519459 | Arthrex® | ARTHREX, INC. | MDM | 2026-03-16 |
| 00888867519473 | Arthrex® | ARTHREX, INC. | MDM | 2026-03-16 |
| 00888867519503 | Arthrex® | ARTHREX, INC. | MDM | 2026-03-16 |
| 00888867519510 | Arthrex® | ARTHREX, INC. | MDM | 2026-03-16 |
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| 00888867529793 | Arthrex® | ARTHREX, INC. | MDM | 2026-03-16 |
| 00198506089510 | ELMED INCORPORATED | ELMED INCORPORATED | MDM | 2026-03-13 |
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