510(k) clearances

CYLOX® ST

Signus Medizintechnik GmbH · Orthopedic

K243188Substantially EquivalentTraditionalOVE
Open FDA's page for this record
Third party flag
N
City
Alzenau
Advisory committee description
Orthopedic
Address 1
Industriestrasse 2
Statement or summary
Summary
Product code
OVE
Zip code
D-63755
Applicant
Signus Medizintechnik GmbH
Decision date
2025-02-11
Decision code
SESE
Country code
DE
Device name
CYLOX® ST
Advisory committee
OR
Contact
Antje Schmidt
K number
K243188
Date received
2024-09-30
Review advisory committee
OR
Postal code
D-63755
Decision description
Substantially Equivalent
Clearance type
Traditional
Harmonized identifiers (openFDA)
Device name
Intervertebral Fusion Device With Integrated Fixation, Cervical
Medical specialty description
Orthopedic
Regulation number
888.3080
Device class
2
Registration number
3007766698, 9610612, 9617297, 3018094310, 1000432246, 3005739886, 3017521423, 3008868758, 3007604895, 8020776, 1057425, 8043792, 3015876273, 3015877656, 1226544, 2532027, 1724955, 3010047402, 3005180920, 3005706667, 3007125392, 3015212339, 3007993775, 3007485169, 2134285, 3009051471, 3008864603, 3005977257, 3009887475, 3019837678, 3006846753, 3030412764, 3003477135, 3015216945, 3010866843, 3013820501, 3009554293, 3033509898, 3008812560, 3006017180 +206 more
FEI number
3007766698, 1000477302, 3018094310, 1000432246, 3000718490, 3017521423, 3008868758, 3007604895, 3005739886, 3015876273, 3015877656, 4224, 3001237338, 3003058119, 3010047402, 3005180920, 3005706667, 3007125392, 3015212339, 3007993775, 1000139987, 3002808269, 3007485169, 1000306303, 3009051471, 3008864603, 3005977257, 3009887475, 3019837678, 3011764740, 3006846753, 3003015552, 3030412764, 3003477135, 3015216945, 3002929183, 3010866843, 3003690049, 3013820501, 3009554293 +206 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.