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

THE C-S DISTRACTION ROD ASSEMBLY

K Number: K890187 · Decision Apr 6, 1989
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
95
Review Days
78

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
THE C-S DISTRACTION ROD ASSEMBLY
K Number
K890187
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Orthopedic Systems, Inc.
Date Received
January 18, 1989
Decision Date
April 6, 1989
Product Code
KWP
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
KWP Appliance, Fixation, Spinal Interlaminal

Similar 510(k) Clearances

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

View all

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. →