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

VILEX BONE PLATE SYSTEM

K Number: K041287 · Decision Aug 5, 2004
Classifications
1
FEI Numbers
653
Registration Numbers
653
Same Product Code
1040
Applicant Total
13
Review Days
84

Basic Information

Device Name
VILEX BONE PLATE SYSTEM
K Number
K041287
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
VILEX, INC.
Date Received
May 13, 2004
Decision Date
August 5, 2004
Product Code
HWC
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
HWC Screw, Fixation, Bone

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HWC), 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
K052196 VILEX X-FIX
K041289 TALUS OF VILEX (TOV)
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. →