FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CONCEPT POWER SYSTEM

K Number: K881954 · Decision Nov 9, 1988
Classifications
1
FEI Numbers
67
Registration Numbers
67
Same Product Code
55
Applicant Total
83
Review Days
183

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Basic Information

Device Name
CONCEPT POWER SYSTEM
K Number
K881954
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Concept, Inc.
Date Received
May 10, 1988
Decision Date
November 9, 1988
Product Code
HSZ
Advisory Committee
General, Plastic Surgery
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
HSZ Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/Attachment

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Other Clearances by Concept, Inc.

K Number Device Name
K912640 CONCEPT ENDOSTEAL FIXATION DEVICE
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
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. →