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

SOFT TISSUE EXPANDER

K Number: K923381 · Decision May 5, 1993
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
8
Applicant Total
78
Review Days
300

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Basic Information

Device Name
SOFT TISSUE EXPANDER
K Number
K923381
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Acufex Microsurgical, Inc.
Date Received
July 9, 1992
Decision Date
May 5, 1993
Product Code
HWQ
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
HWQ Passer

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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. →