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

F20

K Number: K103433 · Decision Jan 3, 2011
Classifications
1
FEI Numbers
112
Registration Numbers
112
Same Product Code
106
Applicant Total
11
Review Days
40

Basic Information

Device Name
F20
K Number
K103433
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3027
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
TEKNIMED SA
Date Received
November 24, 2010
Decision Date
January 3, 2011
Product Code
NDN
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
NDN Cement, Bone, Vertebroplasty

Similar 510(k) Clearances

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

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Other Clearances by TEKNIMED SA

K Number Device Name
K090435 VERTECEM
K083005 NANGEL
K080873 OPACITY + BONE CEMENT
K062102 ODONCER
K043593 SPINE-FIX BIOMIMETIC BONE CEMENT
K042911 CEMENTEK LV
K041493 CEMENTEK
K040669 CERAFORM BONE VOID FILLER
K031826 TRIHA +
K032685 CEMSTOP CEMENT RESTRICTOR
Search all 11 clearances from TEKNIMED SA →