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

CONCEPT ENDOSTEAL FIXATION DEVICE

K Number: K912640 · Decision May 1, 1992
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
83
Review Days
322

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Basic Information

Device Name
CONCEPT ENDOSTEAL FIXATION DEVICE
K Number
K912640
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Concept, Inc.
Date Received
June 14, 1991
Decision Date
May 1, 1992
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

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Other Clearances by Concept, Inc.

K Number Device Name
K912957 CONCEPT MICROMILL
K896648 CONCEPT UNICOMPARTMENTAL KNEE SYSTEM
K894929 STAPLE FIXATION SYSTEM
K892376 INTRAVISION(TM) ARTHROSCOPE SYSTEM (ADD'L APPLI.)
K891109 PANDA(R) NEEDLE CATHETER JEJUNOSTOMY TUBE
K881954 CONCEPT POWER SYSTEM
K884255 CONCEPT CCT-5200, THERMAL THERAPY SYSTEM
K882121 C-FLO SUCTION TUBE
K880414 TENDON HARVESTER
K874676 INTERFERENCE SCREW
Search all 83 clearances from Concept, Inc. →