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

FIREBIRD SPINAL FIXATION SYSTEM

K Number: K130176 · Decision Mar 28, 2013
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
3
Review Days
62

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Basic Information

Device Name
FIREBIRD SPINAL FIXATION SYSTEM
K Number
K130176
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthofix
Date Received
January 25, 2013
Decision Date
March 28, 2013
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.

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Other Clearances by Orthofix

K Number Device Name
K122901 FIREBIRD SPINAL FIXATION SYSTEM, PHOENIX MIS SPINAL FIXATION SYSTEM
K121649 CONSTRUX MINI PEEK TI SPACER SYSTEM