OGmend Implant System— 510(k) DEN180065
UnknownWoven Orthopedic Technologies, LLC
FDA 510(k) clearance DEN180065 for OGmend Implant System, Unknown on 2020-05-01. Applicant: Woven Orthopedic Technologies, LLC. Device class: 2.
Clearance details
- Applicant
- Woven Orthopedic Technologies, LLC
- Product code
- Code QAC
- Device class
- Class 2
- Regulation
- 21 CFR 888.3043
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Manchester, CT, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.