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

STERISPINE CC

K Number: K162531 · Decision Dec 29, 2016
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
161
Applicant Total
13
Review Days
111

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Basic Information

Device Name
STERISPINE CC
K Number
K162531
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Safe Orthopaedics
Date Received
September 9, 2016
Decision Date
December 29, 2016
Product Code
OVE
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
OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OVE), 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
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 13 clearances from Safe Orthopaedics →