K242263
- 510(k) number
- K242263
- Device name
- TECHFIT DISRP® System
- Applicant
- Techfit Digital Surgery, Inc. FL · US
- Product code
- DZJ — Driver, Wire, And Bone Drill, Manual
- Decision date
- 2024-12-11
- Date received
- 2024-08-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K242263.pdf
Official FDA record: K242263
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.