CoLink
- Primary DI
- 00810021863887
- Brand
- CoLink
- Company
- In2Bones USA, LLC
- Model
- P04 N0361
- Catalog number
- P04 N0361
- Device description
- COLINK 2 H-PLATE TRIAL, SMALL, NON-STERILE
- Published
- 2026-03-27
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Rx
- true
- OTC
- 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 |
|---|---|
| K163293 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00810021864969 | Previous | GS1 | 0 | |
| 00810021863887 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00810021864969 | 00810021864969 | 810021864969 | 0810021864969 |
| 00810021863887 | 00810021863887 | 810021863887 | 0810021863887 |
GMDN Terms#
| Term | Definition |
|---|---|
| Surgical drill guide, reusable | A manual surgical device designed to simultaneously place, angle, and guide a rotating surgical drill on hard tissue (e.g., bone); some types are also intended for guiding bone-coring instruments (e.g., keel punch). It is designed in a tubular form or with guiding holes and may have serrations at its distal end to enable firm placement on hard tissue surfaces (it is not bored into the tissue); it can have a handle or be held by another device (e.g., orthopaedic jig), and typically allows protection of the surrounding soft tissue during surgery. It is typically made of metal and may have graduations along its length; it is not custom-made for a specific patient. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(866)426-6633 | CustomerExperience@conmed.com |
Regulatory Flags#
- DUNS number
- 079700711
- Device count
- 1
- Lot or batch
- true
- Manufacturing date on label
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00810021861173 | 5MS | P06 N0241 | P06 N0241 | 2019-06-14 |
| 00817906029734 | 5MS | P06 N0261 | P06 N0261 | 2019-06-14 |
| 00817906029741 | 5MS | P06 N0271 | P06 N0271 | 2019-06-14 |
| 00817906029758 | 5MS | P06 N0281 | P06 N0281 | 2019-06-14 |
| 00817906029765 | 5MS | P06 N0291 | P06 N0291 | 2019-06-14 |
| 00817906027921 | CoLink | P04 N0012 | P04 N0012 | 2018-10-22 |
| 00817906027945 | CoLink | P04 N0101 | P04 N0101 | 2018-10-22 |
| 00817906027952 | CoLink | P04 N0102 | P04 N0102 | 2018-10-22 |
| 00817906027969 | CoLink | P04 N0103 | P04 N0103 | 2018-10-22 |
| 00817906027976 | CoLink | P04 N0104 | P04 N0104 | 2018-10-22 |
| 00817906027983 | CoLink | P04 N0105 | P04 N0105 | 2018-10-22 |
| 00817906027990 | CoLink | P04 N0131 | P04 N0131 | 2018-10-22 |
| 00817906028003 | CoLink | P04 N0132 | P04 N0132 | 2018-10-22 |
| 00817906028010 | CoLink | P04 N0141 | P04 N0141 | 2018-10-22 |
| 00817906028027 | CoLink | P04 N0142 | P04 N0142 | 2018-10-22 |
| 00817906028034 | CoLink | P04 N0151 | P04 N0151 | 2018-10-22 |
| 00817906028041 | CoLink | P04 N0152 | P04 N0152 | 2018-10-22 |
| 00817906028058 | CoLink | P04 N0161 | P04 N0161 | 2018-10-22 |
| 00817906028065 | CoLink | P04 N0171 | P04 N0171 | 2018-10-22 |
| 00817906028072 | CoLink | P04 N0172 | P04 N0172 | 2018-10-22 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00190376544496 | Invictus | ALPHATEC SPINE, INC. | FZX | 2026-07-30 |
| 03701089528054 | AMPLITUDE | AMPLITUDE SAS | FZX | 2026-07-29 |
| 03701089542548 | AMPLITUDE | AMPLITUDE SAS | FZX | 2026-07-29 |
| 03701089543316 | AMPLITUDE | AMPLITUDE SAS | FZX | 2026-07-29 |
| 03701089543330 | AMPLITUDE | AMPLITUDE SAS | FZX | 2026-07-29 |
| 03701089543354 | AMPLITUDE | AMPLITUDE SAS | FZX | 2026-07-29 |
| 03701089543378 | AMPLITUDE | AMPLITUDE SAS | FZX | 2026-07-29 |
| 03701089543682 | AMPLITUDE | AMPLITUDE SAS | FZX | 2026-07-29 |
| 03700569674335 | Newclip Instruments | NEWCLIP TECHNICS | FZX | 2026-07-28 |
| 03700569674342 | Newclip Instruments | NEWCLIP TECHNICS | FZX | 2026-07-28 |
| 03700569674281 | Newclip Instruments | NEWCLIP TECHNICS | FZX | 2026-07-27 |
| 03700569674298 | Newclip Instruments | NEWCLIP TECHNICS | FZX | 2026-07-27 |
| 00842188132568 | Tools-AFS | Trimed, INC. | FZX | 2026-07-24 |
| 00841731153128 | ARTEMIS FUZE | VILEX LLC | FZX | 2026-07-22 |
| 00888118147226 | LEVEL ONE EXTREMITY | KLS-Martin L.P. | FZX | 2026-07-21 |
| 00888118147233 | LEVEL ONE EXTREMITY | KLS-Martin L.P. | FZX | 2026-07-21 |
| 00888118147240 | LEVEL ONE EXTREMITY | KLS-Martin L.P. | FZX | 2026-07-21 |
| 00888118147257 | LEVEL ONE EXTREMITY | KLS-Martin L.P. | FZX | 2026-07-21 |
| 00888118147264 | LEVEL ONE EXTREMITY | KLS-Martin L.P. | FZX | 2026-07-21 |
| 00888118147271 | LEVEL ONE EXTREMITY | KLS-Martin L.P. | FZX | 2026-07-21 |
| 00888118147714 | LEVEL ONE EXTREMITY | KLS-Martin L.P. | FZX | 2026-07-21 |
| 00888118147721 | LEVEL ONE EXTREMITY | KLS-Martin L.P. | FZX | 2026-07-21 |
| 00888118147738 | LEVEL ONE EXTREMITY | KLS-Martin L.P. | FZX | 2026-07-21 |
| 00888118147745 | LEVEL ONE EXTREMITY | KLS-Martin L.P. | FZX | 2026-07-21 |
| 00810111228374 | Positioner / Compressor | Treace Medical Concepts, Inc. | FZX | 2026-07-17 |
| 00810111228381 | Positioner / Compressor | Treace Medical Concepts, Inc. | FZX | 2026-07-17 |
| 18257200131198 | Firebird SI Fusion | Orthofix US LLC | FZX | 2026-07-17 |
| 18257200131204 | Firebird SI Fusion | Orthofix US LLC | FZX | 2026-07-17 |
| 18257200131235 | Firebird SI Fusion | Orthofix US LLC | FZX | 2026-07-17 |
| 18257200131334 | Firebird SI Fusion | Orthofix US LLC | FZX | 2026-07-17 |