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

SPINAL CONCEPTS INC. PATHFINDER

K Number: K030625 · Decision Mar 28, 2003
Classifications
1
FEI Numbers
413
Registration Numbers
413
Same Product Code
873
Applicant Total
33
Review Days
29

Basic Information

Device Name
SPINAL CONCEPTS INC. PATHFINDER
K Number
K030625
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SPINAL CONCEPTS, INC.
Date Received
February 27, 2003
Decision Date
March 28, 2003
Product Code
NKB
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
NKB Thoracolumbosacral Pedicle Screw System

Similar 510(k) Clearances

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

View all

Other Clearances by SPINAL CONCEPTS, INC.

K Number Device Name
K051000 FORTITUDE VUE VERTEBRAL BODY REPLACEMENT DEVICE
K050706 HARMONY PORT SYSTEM, MODEL 1907 SERIES
K040096 SPINAL CONCEPTS, INC. TANDEM SPINOUS PROCESS PLATE SYSTEM
K033663 SPINAL CONCEPTS INC. CODA
K033517 SPINAL CONCEPTS INC. CADENCE AND TRAXIS
K031855 SPINAL CONCEPTS, INC. INSIGHT PEDICLE SCREW SYSTEM
K031985 SPINAL CONCEPTS INC. NEX-LINK SPINAL FIXATION SYSTEM
K031318 TRAXIS CEMENT RESTRICTOR
K031672 SPINAL CONCEPTS, INC. INFIX SYSTEM
K031837 MODIFICATION TO FORTITUDE CEMENT RESTRICTOR
Search all 33 clearances from SPINAL CONCEPTS, INC. →