Fortilink-C IBF System
- Primary DI
- 00846468099732
- Brand
- Fortilink-C IBF System
- Company
- Pioneer Surgical Technology, Inc.
- Model
- 65-C-TRL-M-6-10L
- Catalog number
- 65-C-TRL-M-6-10L
- Device description
- TRIAL SPACER
- Published
- 2021-08-19
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| HWT | TEMPLATE |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HWT | Template | Orthopedic | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00846468099732 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00846468099732 | 00846468099732 | 846468099732 | 0846468099732 |
GMDN Terms#
| Term | Definition |
|---|---|
| Surgical implant template, reusable | A device designed to determine the appropriate size and placement of a non-dental implant for a patient prior to or during implantation surgery. It is typically available as a graduated set or an individual plate (e.g., a translucent plastic sheet or a cut metal shape) with patterns/sizes corresponding to the size of the implant to be used to aid the surgeon in final selection of implant size, placement, and/or adaption. It is used for, e.g., total- or partial-joint prostheses, bone fracture fixation implants (plates, nails, including skull plate implants) or other types of surgical implants. This is a reusable device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(386)418-8888 | labeling@rtix.com |
| +1(906)226-9909 | labeling@resolvesurg.com |
| +1(906)226-9909 | regulatory@exalta.com |
Regulatory Flags#
- DUNS number
- 793384496
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
- Sterilization required before use
- true
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| 00840298703708 | CODA™ Anterior Cervical Plate System | 58-202230014S | 2022-30-014S | 2023-06-28 |
| 00840298701445 | CODA™ Anterior Cervical Plate System | 58-102201010S | 1022-01-010S | 2023-06-26 |
| 00840298701452 | CODA™ Anterior Cervical Plate System | 58-102201012S | 1022-01-012S | 2023-06-26 |
| 00840298701469 | CODA™ Anterior Cervical Plate System | 58-102201014S | 1022-01-014S | 2023-06-26 |
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| 00840298701490 | CODA™ Anterior Cervical Plate System | 58-102201020S | 1022-01-020S | 2023-06-26 |
| 00840298701506 | CODA™ Anterior Cervical Plate System | 58-102201022S | 1022-01-022S | 2023-06-26 |
| 00840298701520 | CODA™ Anterior Cervical Plate System | 58-102201026S | 1022-01-026S | 2023-06-26 |
| 00840298701537 | CODA™ Anterior Cervical Plate System | 58-102201028S | 1022-01-028S | 2023-06-26 |
| 00840298701544 | CODA™ Anterior Cervical Plate System | 58-102201030S | 1022-01-030S | 2023-06-26 |
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| 00840298701582 | CODA™ Anterior Cervical Plate System | 58-102202030S | 1022-02-030S | 2023-06-26 |
| 00840298701599 | CODA™ Anterior Cervical Plate System | 58-102202032S | 1022-02-032S | 2023-06-26 |
| 00840298701605 | CODA™ Anterior Cervical Plate System | 58-102202034S | 1022-02-034S | 2023-06-26 |
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| 00840298701629 | CODA™ Anterior Cervical Plate System | 58-102202038S | 1022-02-038S | 2023-06-26 |
| 00840298701636 | CODA™ Anterior Cervical Plate System | 58-102202040S | 1022-02-040S | 2023-06-26 |
| 00840298701643 | CODA™ Anterior Cervical Plate System | 58-102202042S | 1022-02-042S | 2023-06-26 |
| 00840298701650 | CODA™ Anterior Cervical Plate System | 58-102202044S | 1022-02-044S | 2023-06-26 |
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