NovoGen Wound Matrix— 510(k) K220498
Substantially EquivalentNovabone Products, LLC
FDA 510(k) clearance K220498 for NovoGen Wound Matrix, Substantially Equivalent on 2023-06-09. Applicant: Novabone Products, LLC. Device class: Unclassified.
Clearance details
- Applicant
- Novabone Products, LLC
- Product code
- Code KGN
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Alachua, FL, US
Recent devices under product code KGN
view allMore clearances from Novabone Products, LLC
view all- K242299 — NovaBone Putty - Synthetic Bioactive Bone Graft
- K240404 — NovaBone Putty - Bioactive Synthetic Bone Graft (NB6600, NB6610, NB6615)
- K163310 — NovaBone IRM
- K152071 — NovaBone MacroFORM MIS Composite - 2.5cc, NovaBone MIS Cartridge Delivery System (cartridge handle only)
- K142712 — Dental Collagen Wound Dressing (Nova Tape and NovaPlug)
Adverse events under product code KGN
product code KGN- Other
- 2
- Total
- 2
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.