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

OEC/REZAIAN SPINAL FIXATOR

K Number: K841189 · Decision May 16, 1984
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
45
Review Days
57

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Basic Information

Device Name
OEC/REZAIAN SPINAL FIXATOR
K Number
K841189
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Orthopedic Equipment Co., Inc.
Date Received
March 20, 1984
Decision Date
May 16, 1984
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

Similar 510(k) Clearances

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Other Clearances by Orthopedic Equipment Co., Inc.

K Number Device Name
K834035 UNIVERSAL SELF-ALIGNING ACETABULAR COM
K800530 SCHLEIN TRI-SURFACE ANKLE
K781445 SPREADER
K790247 TOURNIQUET TEST GAGE
K790209 FILTER SYSTEM, ALTNER DISPOSABLE
K781450 DRIVERS
K781444 OUTRIGGER DISTRACTION UNIT
K781451 FLAT WRENCH
K781447 THREADED ROD CLAMP
K781449 HARRINGTON SPINAL ELEVATOR
Search all 45 clearances from Orthopedic Equipment Co., Inc. →