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

CRUCIOMETER

K Number: K884483 · Decision Jan 18, 1989
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
0
Applicant Total
95
Review Days
85

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Basic Information

Device Name
CRUCIOMETER
K Number
K884483
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.4420
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Orthopedic Systems, Inc.
Date Received
October 25, 1988
Decision Date
January 18, 1989
Product Code
JZE
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JZE Spoon, Ear

Other Clearances by Orthopedic Systems, Inc.

K Number Device Name
K952495 ANCHORS AWAY SOFT TISSUE ATTACHMENT SYSTEM
K920256 SPINE MOTION ANALYZER WITH EMG
K910736 JACKSON MULTIPURPOSE OPERATING TABLE
K910031 PARK CITY SHOULDER POSITIONER
K903938 C FIT CUP
K892503 NUFFIELD TOTAL KNEE
K896678 SILICONE PLUG
K894283 COMPREHENSIVE SPINE MOTION ANALYZER
K890498 FREEMAN MODULAR HIP STEM RIDGED VERSION
K890331 FREEMAN TOTAL HIP SYSTEM RIDGED STEM
Search all 95 clearances from Orthopedic Systems, Inc. →