4CIS Chiron Spinal Fixation System— 510(k) K203233
Substantially EquivalentSolco Biomedical Co., Ltd.
FDA 510(k) clearance K203233 for 4CIS Chiron Spinal Fixation System, Substantially Equivalent on 2022-06-01. Applicant: Solco Biomedical Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Solco Biomedical Co., Ltd.
- Product code
- Code NKB
- Device class
- Class 2
- Regulation
- 21 CFR 888.3070
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Pyeongtaek-Si, KR
Recent devices under product code NKB
view all- K262828 — KHEIRON® Spinal Fixation System, including patient specific K-ROD
- K253943 — Tiger 2 System
- K260362 — QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration)
- K261284 — Invictus® Small Stature Spinal Fixation System; Invictus® 2.0 Spinal Fixation System
- K253802 — KHEIRON® Spinal Fixation System, including patient specific K-ROD
More clearances from Solco Biomedical Co., Ltd.
view all- K231655 — 4CIS® Chiron Spinal Fixation System
- K192044 — 4CIS Marlin PEEK ACIF Cage
- K190563 — 4CIS PEEK PLIF Cage, 4CIS Pebble Beach PEEK PLIF Cage, 4CIS Torrey Pines PEEK TLIF Cage, 4CIS Dunes PEEK DLIF Cage, 4CIS Augusta PEEK ALIF Cage
- K190471 — 4CIS® Chiron Spinal Fixation System
- K182489 — 4CIS® Pinehurst Anterior Cervical Plate system
Adverse events under product code NKB
product code NKB- Death
- 27
- Injury
- 5,033
- Malfunction
- 4,140
- Total
- 9,200
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.