SYNTHES LIMITED CONTACT-DYNAMIC HIP SCREW IMPLANT— 510(k) K923613
Substantially EquivalentSynthes (Usa)
FDA 510(k) clearance K923613 for SYNTHES LIMITED CONTACT-DYNAMIC HIP SCREW IMPLANT, Substantially Equivalent on 1993-06-22. Applicant: Synthes (Usa). Device class: 2.
Clearance details
- Applicant
- Synthes (Usa)
- Product code
- Code JDO
- Device class
- Class 2
- Regulation
- 21 CFR 888.3030
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Paoli, PA, US
Recent devices under product code JDO
view all- K230764 — OsteoCentric Integrated Hip Fastener System
- K213126 — Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc, D-Rad, TC-100, VLP Mini-Mod, Compression Hip Screw (CHS), CONQUEST FN, and cannulated screws
- K210247 — OsteoCentric Integrated Hip Fastener System
- K193029 — CONQUEST FN
- K173826 — THP Hip Fracture Plating System
More clearances from Synthes (Usa)
view all- K141527 — DEPUY SYNTHES VARIABLE ANGLE LOCKING HAND SYSTEM
- K131984 — SYNTHES SYNSONIC ULNA NAIL
- K121601 — SYNTHES 2.7/3.5MM VARIABLE ANGLE LCP ANKLE TRAUMA SYSTEM-ANTEROLATERAL DISTAL TIBIA PLATE
- K120854 — SYNTHES VA LCP ANKLE TRAUMA SYSTEM
- K120717 — SYNTHES VARIABLE ANGLE LCP ELBOW SYSTEM (MEDICAL AND POSTEROLATERAL DISTAL HUMERUS PLATES)
Data sourced from openFDA. This site is unofficial and independent of the FDA.