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

CANNULATED MALLEOLAR SCREW

K Number: K931682 · Decision Apr 5, 1994
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
47
Review Days
365

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Basic Information

Device Name
CANNULATED MALLEOLAR SCREW
K Number
K931682
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Onyx Medical Corp.
Date Received
April 5, 1993
Decision Date
April 5, 1994
Product Code
KWK
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
KWK Appliance, Nail/Blade/Plate Combination, Single Component

Other Clearances by Onyx Medical Corp.

K Number Device Name
K942022 FACE-IT SHIELD
K931690 SPOON PLATE
K934614 MINI FRAGMENT PLATE
K931692 T-PLATE
K931684 EPIPHYSIS PLATE
K931680 CANNULATED CANCELLOUS SCREW
K931679 BUTTRESS PLATE
K934615 CANCELLOUS BONE SCREW
K931683 CLOVERLEAF PLATE
K931693 1/3 TUBULAR PLATE
Search all 47 clearances from Onyx Medical Corp. →