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

CONCEPT CURETTE

K Number: K862657 · Decision Jul 23, 1986
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
669
Applicant Total
83
Review Days
9

Basic Information

Device Name
CONCEPT CURETTE
K Number
K862657
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
CONCEPT, INC.
Date Received
July 14, 1986
Decision Date
July 23, 1986
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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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
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