KAPP CUSTOM ULNAR HEAD WRIST IMPLANT— 510(k) K033930
Substantially EquivalentKapp Surgical Instrument, Inc.
FDA 510(k) clearance K033930 for KAPP CUSTOM ULNAR HEAD WRIST IMPLANT, Substantially Equivalent on 2004-07-28. Applicant: Kapp Surgical Instrument, Inc.. Device class: 2.
Clearance details
- Applicant
- Kapp Surgical Instrument, Inc.
- Product code
- Code KXE
- Device class
- Class 2
- Regulation
- 21 CFR 888.3810
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Warrensville, OH, US
Recent devices under product code KXE
view allMore clearances from Kapp Surgical Instrument, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.