FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

STERISPINEPS PEDICLE SCREW, STERISPINEPS ROD

K Number: K121299 · Decision Jul 30, 2012
Classifications
1
FEI Numbers
413
Registration Numbers
413
Same Product Code
873
Applicant Total
12
Review Days
91

Basic Information

Device Name
STERISPINEPS PEDICLE SCREW, STERISPINEPS ROD
K Number
K121299
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SAFE ORTHOPAEDICS
Date Received
April 30, 2012
Decision Date
July 30, 2012
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 SAFE ORTHOPAEDICS

K Number Device Name
K170528 Sterispine™ PS
K162531 STERISPINE CC
K151921 STERISPINE PS
K151747 STERISPINE PS
K151756 STERISPINE LC CAGE
K150092 STERISPINE PS Pedicle Screw
K140802 STERISPINE PS
K133893 STERISPINE LC CAGE
K130632 STERISPINE PS PEDICLE SCREW
K122021 STERISPINE LC CAGE
Search all 12 clearances from SAFE ORTHOPAEDICS →