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

MET-HEAD MODEL# MHDD-XX:CC DIAMETER, CC CANNULATION

K Number: K070052 · Decision Mar 28, 2007
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
45
Applicant Total
13
Review Days
83

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Basic Information

Device Name
MET-HEAD MODEL# MHDD-XX:CC DIAMETER, CC CANNULATION
K Number
K070052
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3730
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vilex, Inc.
Date Received
January 4, 2007
Decision Date
March 28, 2007
Product Code
KWD
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
KWD Prosthesis, Toe, Hemi-, Phalangeal

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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
K052196 VILEX X-FIX
K041287 VILEX BONE PLATE SYSTEM
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
K991151 VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW, ORTHEX CANNULATED BONE SCREW
Search all 13 clearances from Vilex, Inc. →