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

K-CAPE ORTHOPEDIC WIRES AND PINS

K Number: K901525 · Decision Apr 23, 1990
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
403
Applicant Total
4
Review Days
21

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Basic Information

Device Name
K-CAPE ORTHOPEDIC WIRES AND PINS
K Number
K901525
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Westcon Orthopedics, Inc.
Date Received
April 2, 1990
Decision Date
April 23, 1990
Product Code
KTT
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
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

Similar 510(k) Clearances

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

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Other Clearances by Westcon Orthopedics, Inc.

K Number Device Name
K914812 K-CAP-E, STERILE
K912762 K-CAP-I, STERILE
K902053 K-CAP-I ORTHOPEDIC FIXATION WIRE CAP