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

CORB TM COUNTERROTATING BIOPSY NEEDLE

K Number: K811005 · Decision Jun 15, 1981
Classifications
1
FEI Numbers
67
Registration Numbers
67
Same Product Code
55
Applicant Total
376
Review Days
62

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Basic Information

Device Name
CORB TM COUNTERROTATING BIOPSY NEEDLE
K Number
K811005
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Zimmer, Inc.
Date Received
April 14, 1981
Decision Date
June 15, 1981
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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