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

ACUFEX INTRA ARTICULAR MEASURING DEVICE

K Number: K925335 · Decision Dec 29, 1992
Classifications
1
FEI Numbers
372
Registration Numbers
372
Same Product Code
3
Applicant Total
78
Review Days
68

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Basic Information

Device Name
ACUFEX INTRA ARTICULAR MEASURING DEVICE
K Number
K925335
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4300
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Acufex Microsurgical, Inc.
Date Received
October 22, 1992
Decision Date
December 29, 1992
Product Code
HTJ
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
HTJ Gauge, Depth

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HTJ), ordered by most recent decision date.

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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. →