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

C-TEK C-THRU ANTERIOR CERVICAL PLATE SYSTEM

K Number: K041794 · Decision Jul 19, 2004
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
39
Review Days
17

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Basic Information

Device Name
C-TEK C-THRU ANTERIOR CERVICAL PLATE SYSTEM
K Number
K041794
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Interpore Cross Intl.
Date Received
July 2, 2004
Decision Date
July 19, 2004
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

Similar 510(k) Clearances

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

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Other Clearances by Interpore Cross Intl.

K Number Device Name
K050861 PEEK CAS
K031399 INTERGRO DBM
K041407 TITANIUM MESH IMPLANT
K043229 MODIFICATION TO ALTIUS OCT SYSTEM
K042798 C-TEK C-TRUN ANTERIOR CERVICAL PLATE SYSTEM
K040928 EXPANDABLE PEEK VBR IMPLANT
K041449 SYNERGY HELICAL FLANGE PLUG, HELICAL FLANGE SEAT AND HELICAL FLANGE REDUCTION SEAT
K033961 ALTIUS OCT SYSTEM
K040168 MODIFICATION TO GEO STRUCTURE
K031772 TI FENESTRATED PLATE
Search all 39 clearances from Interpore Cross Intl. →