Kirschner wire
- Primary DI
- 03760225715499
- Brand
- Kirschner wire
- Company
- IN2BONES
- Model
- K20 NS150
- Catalog number
- K20 NS150
- Device description
- PIT'STOP POSITIONING GUIDE DIAM 1.6MM– LG.150MM
- Published
- 2016-03-18
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| FZX | Guide, surgical, instrument |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| FZX | Guide, Surgical, Instrument | General, Plastic Surgery | 1 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K153204 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 03760225715499 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 03760225715499 | 03760225715499 | 3760225715499 |
GMDN Terms#
| Term | Definition |
|---|---|
| Orthopaedic bone pin, non-bioabsorbable | A thin, implantable rod intended to be used for the stabilization of a bone fracture or bone grafts, or for an osteotomy or arthrodesis (internal and/or external fixation). It is typically drilled into bone and may be smooth or threaded, solid or cannulated, and/or semi-flexible. Also known as a Kirschner-wire (K-wire), it may in addition be intended to assist with the introduction of a surgical instrument and/or implant; it is not intended for implantation into the intramedullary canal (i.e., not a nail). It is made of a non-bioabsorbable material (e.g., stainless steel). Some designs may have a break-off shank and/or be coated to improve long-term fixation. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Length | 0 | |
| Outer Diameter | 0 |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(866)426-6633 | CustomerExperience@conmed.com |
Regulatory Flags#
- DUNS number
- 263616749
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- 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
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 03760225710968 | IBS™ | G01 00852 | G01 00852 | 2020-06-11 |
| 03760225710975 | NEOFUSE | G01 00862 | G01 00862 | 2020-06-11 |
| 03760225711002 | NEOFUSE | G01 00891 | G01 00891 | 2020-06-11 |
| 03760225713129 | IBS™ | G01 00411 | G01 00411 | 2020-06-11 |
| 03760225714263 | IBS™ | G01 00421 | G01 00421 | 2020-06-11 |
| 03760225717004 | NEOFUSE | P02 00081 | P02 00081 | 2019-07-17 |
| 03760225717011 | NEOFUSE | P02 00071 | P02 00071 | 2019-07-17 |
| 03760225717110 | NEOFUSE | P02 00171 | P02 00171 | 2019-07-17 |
| 03760225717172 | NEOFUSE | P02 00011 | P02 00011 | 2019-07-17 |
| 03760225717189 | NEOFUSE | P02 00021 | P02 00021 | 2019-07-17 |
| 03760225717219 | NEOFUSE | P02 00051 | P02 00051 | 2019-07-17 |
| 03701337606800 | NEOFUSE | P02 00301 | P02 00301 | 2022-05-10 |
| 03760225713167 | IBS™ | G01 01271 | G01 01271 | 2022-05-09 |
| 03760225713174 | IBS™ | G01 01261 | G01 01261 | 2022-05-09 |
| 03760225713181 | IBS™ | G01 01251 | G01 01251 | 2022-05-09 |
| 03760225714287 | IBS™ | G01 01291 | G01 01291 | 2022-05-09 |
| 03760225714294 | IBS™ | G01 01301 | G01 01301 | 2022-05-09 |
| 03760225714300 | IBS™ | G01 01311 | G01 01311 | 2022-05-09 |
| 03760225717127 | NEOFUSE | G01 01561 | G01 01561 | 2020-06-09 |
| 03760225717141 | NEOFUSE | G01 01571 | G01 01571 | 2020-06-09 |
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