FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

CYLOX® ST

K Number: K243188 · Decision Feb 11, 2025
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
161
Applicant Total
23
Review Days
134

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Basic Information

Device Name
CYLOX® ST
K Number
K243188
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Signus Medizintechnik GmbH
Date Received
September 30, 2024
Decision Date
February 11, 2025
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

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Other Clearances by Signus Medizintechnik GmbH

K Number Device Name
K241438 Signus Tetris™ St; Signus Tetris™ R St
K220658 COSY Cervicothoracic Occipital Rod-Screw System
K212755 SIGNUS SACRONAIL® Transsacral Stabilization System
K151704 Diplomat® Spinal System
K141405 MOBIS II ST SPINAL IMPLANT
K123758 TASMIN R
K131372 MOBIS II
K122317 TETRIS II
K111792 MOBIS, MOVAL, SEMIAL, TETRISMODEL PEEK AND TITANIUM, KIMBA MODEL STANDARD AND MINI
K090387 KAINOS+
Search all 23 clearances from Signus Medizintechnik GmbH →