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

ACUFEX DREZ COMMUNICATING DRILL GUIDE

K Number: K834350 · Decision Mar 19, 1984
Classifications
1
FEI Numbers
526
Registration Numbers
526
Same Product Code
18
Applicant Total
78
Review Days
97

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Basic Information

Device Name
ACUFEX DREZ COMMUNICATING DRILL GUIDE
K Number
K834350
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Acufex Microsurgical, Inc.
Date Received
December 13, 1983
Decision Date
March 19, 1984
Product Code
FZX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FZX Guide, Surgical, Instrument

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Other Clearances by Acufex Microsurgical, Inc.

K Number Device Name
K961555 ACUFEX TAG BIOABSORBABLE ANCHORS
K961853 PROLINE FAST PASS ARTHOSCOPIC NEEDLE PASSER
K954246 ACUFEX ENDOFIX ABSORBABLE INTERFERENCE SCREW
K952535 ACUFEX ENDOBUTTON TAPE
K953276 ACUFEX TAG DELIVERY SYSTEM
K953459 ACUFEX TAG ANCHOR
K941740 ACUFEX ROTATOR CUFF FIXATION BUTTON
K944500 ACUFEX PATELLAR BONE BLOCK SIZER
K951859 ACUFEX ENDOBUTTON PACK
K946346 ACUFEX TAG(R) BIOABSORBABLE ANCHORS
Search all 78 clearances from Acufex Microsurgical, Inc. →