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

SIGNUS SACRONAIL® Transsacral Stabilization System

K Number: K212755 · Decision Mar 10, 2022
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
23
Review Days
191

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Basic Information

Device Name
SIGNUS SACRONAIL® Transsacral Stabilization System
K Number
K212755
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Signus Medizintechnik GmbH
Date Received
August 31, 2021
Decision Date
March 10, 2022
Product Code
HWC
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
HWC Screw, Fixation, Bone

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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+
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