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

CONCEPT MICROMILL

K Number: K912957 · Decision Oct 4, 1991
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
83
Review Days
88

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Basic Information

Device Name
CONCEPT MICROMILL
K Number
K912957
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Concept, Inc.
Date Received
July 8, 1991
Decision Date
October 4, 1991
Product Code
HRX
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
HRX Arthroscope

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Other Clearances by Concept, Inc.

K Number Device Name
K912640 CONCEPT ENDOSTEAL FIXATION DEVICE
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. →