Perfix™ Spinal System
- Primary DI
- 08800037560520
- Brand
- Perfix™ Spinal System
- Company
- CG MedTech Co.,Ltd.
- Model
- SH0060
- Published
- 2023-02-25
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Product Codes#
| Code | Name |
|---|---|
| KWP | APPLIANCE, FIXATION, SPINAL INTERLAMINAL |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KWP | Appliance, Fixation, Spinal Interlaminal | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K031595 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 08800037560520 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 08800037560520 | 08800037560520 | 8800037560520 |
GMDN Terms#
| Term | Definition |
|---|---|
| Spinal implant trial | A copy of a final spinal prosthesis, graft, or other implantable spinal device (e.g., may include intervertebral disc prosthesis, spinal cage, spinal hook) used to validate the proper size of the permanent implant required by the patient, to determine its appropriate position, and/or to verify that the implant site has been cut to the proper dimensions. It can be made of metal or plastic. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags#
- DUNS number
- 688811082
- Device count
- 1
- DM exempt
- true
- Lot or batch
- true
- Serial number
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 08800308485811 | ANAX™ OCT SPINAL SYSTEM | OSS0750 | 2026-05-13 | |
| 08800037574725 | Velofix™ SA Cervical Cage | TS0912 | 2026-05-06 | |
| 08800037574732 | Velofix™ SA Cervical Cage | TS0913 | 2026-05-06 | |
| 08800308485804 | ANAX™ OCT Spinal System | OS0090 | 2026-04-21 | |
| 08800247357477 | SECULOK™ ACP SYSTEM | FCA1019 | 2026-03-31 | |
| 08800247357484 | SECULOK™ ACP SYSTEM | FCA1021 | 2026-03-31 | |
| 08800247357491 | SECULOK™ ACP SYSTEM | FCA1023 | 2026-03-31 | |
| 08800247357507 | SECULOK™ ACP SYSTEM | FCA1025 | 2026-03-31 | |
| 08800247357514 | SECULOK™ ACP SYSTEM | FCA1027 | 2026-03-31 | |
| 08800247357521 | SECULOK™ ACP SYSTEM | FCA1029 | 2026-03-31 | |
| 08800247357538 | SECULOK™ ACP SYSTEM | FCA1031 | 2026-03-31 | |
| 08800247357545 | SECULOK™ ACP SYSTEM | FCA1033 | 2026-03-31 | |
| 08800247357552 | SECULOK™ ACP SYSTEM | FCA1035 | 2026-03-31 | |
| 08800247357569 | SECULOK™ ACP SYSTEM | FCA1037 | 2026-03-31 | |
| 08800247357576 | SECULOK™ ACP SYSTEM | FCA1039 | 2026-03-31 | |
| 08800247357583 | SECULOK™ ACP SYSTEM | FCA1041 | 2026-03-31 | |
| 08800247357590 | SECULOK™ ACP SYSTEM | FCA1043 | 2026-03-31 | |
| 08800247357606 | SECULOK™ ACP SYSTEM | FCA1045 | 2026-03-31 | |
| 08800247357613 | SECULOK™ ACP SYSTEM | FCA2031 | 2026-03-31 | |
| 08800247357620 | SECULOK™ ACP SYSTEM | FCA2033 | 2026-03-31 |
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