FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

VILEX X-FIX

K Number: K052196 · Decision Nov 22, 2005
Classifications
1
FEI Numbers
247
Registration Numbers
247
Same Product Code
392
Applicant Total
13
Review Days
103

Basic Information

Device Name
VILEX X-FIX
K Number
K052196
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
VILEX, INC.
Date Received
August 11, 2005
Decision Date
November 22, 2005
Product Code
KTT
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KTT), ordered by most recent decision date.

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Other Clearances by VILEX, INC.

K Number Device Name
K132820 VILEX ULTIMA EXTERNAL FIXATION SYSTEM WITH HA COATED PINS AND WIRES
K112837 VILEX EZ-STAPLE (MEMORY BONE FIXATION STAPLE)
K102413 FUZE: INTRAMEDULLARY INTERNAL FIXATION NAIL
K102401 HEMI IMPLANT; MINI HEMI IMPLANT
K070052 MET-HEAD MODEL# MHDD-XX:CC DIAMETER, CC CANNULATION
K041289 TALUS OF VILEX (TOV)
K041287 VILEX BONE PLATE SYSTEM
K023684 CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ171365
K014154 VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW DB1 THREAD, MODEL F25-XX-09; VILEX SOLID BONE SCREWS DB1 THREAD,MODEL F20-XX-00
K991197 VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW, MODELS P222-XX, S25-XX, P227-XX, S30-XX, P235-XX, S35-XX, P240-XX, S40-XX, P24
Search all 13 clearances from VILEX, INC. →