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

TECHMEDICA I.B.O. BLADE

K Number: K883922 · Decision Dec 8, 1988
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
31
Applicant Total
31
Review Days
83

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Basic Information

Device Name
TECHMEDICA I.B.O. BLADE
K Number
K883922
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4120
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Techmedica, Inc.
Date Received
September 16, 1988
Decision Date
December 8, 1988
Product Code
DZJ
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
DZJ Driver, Wire, And Bone Drill, Manual

Similar 510(k) Clearances

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Other Clearances by Techmedica, Inc.

K Number Device Name
K933935 CKS POROUS COATED FEMORAL COMPONENT
K932017 TECHMEDICA CONTINUUM HIP WITH HA COATING
K931929 TECHMEDICA CONTINUUM HIP SYSTEM
K926387 TECHMEDICA STANDARD CEMENTED HIP SYSTEM
K925420 TECHMEDICA STANDARD BIPOLAR SYSTEM
K923808 MULLER STRAIGHT STEM FEMORAL PROSTHESIS
K926579 TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCRE
K911058 TECHMEDICA CAD/CAM CUSTOM HIP
K925181 TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP
K920080 CONTINUUM KNEE SYSTEM
Search all 31 clearances from Techmedica, Inc. →