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

STERISPINE LC CAGE

K Number: K133893 · Decision Mar 14, 2014
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
13
Review Days
84

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Basic Information

Device Name
STERISPINE LC CAGE
K Number
K133893
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Safe Orthopaedics
Date Received
December 20, 2013
Decision Date
March 14, 2014
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

Similar 510(k) Clearances

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

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Other Clearances by Safe Orthopaedics

K Number Device Name
K201648 Sterispine™ PS
K170528 Sterispine™ PS
K162531 STERISPINE CC
K151921 STERISPINE PS
K151747 STERISPINE PS
K151756 STERISPINE LC CAGE
K150092 STERISPINE PS Pedicle Screw
K140802 STERISPINE PS
K130632 STERISPINE PS PEDICLE SCREW
K122021 STERISPINE LC CAGE
Search all 13 clearances from Safe Orthopaedics →