FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ACUFEX STERILE CANNULATED INTERFERENCE SCREW;

K Number: K900132 · Decision Mar 28, 1990
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
78
Review Days
77

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Basic Information

Device Name
ACUFEX STERILE CANNULATED INTERFERENCE SCREW;
K Number
K900132
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Acufex Microsurgical, Inc.
Date Received
January 10, 1990
Decision Date
March 28, 1990
Product Code
HWC
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
HWC Screw, Fixation, Bone

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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. →