510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K181949Substantially Equivalent

SYMPHONY™ OCT System

Medos International SARL, Lelocle, CH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K181949 is the FDA 510(k) clearance record for SYMPHONY™ OCT System, a class II device, cleared for Medos International SARL on under FDA product code NKG (Posterior Cervical Screw System). FDA's definition for product code NKG reads: "Posterior cervical screw systems are intended for use in fusion procedures of the cervical spine and/or craniocervical junction and/or cervicothoracic junction for: 1) spinal fractures and dislocations; 2) deformities; 3) instabilities; 4)...". FDA records list 101 510(k) clearances for Medos International SARL, from to . As of , FDA records show no recalls naming K181949.

Clearance record

Decision date
Received
(76 days to decision)
Product code
NKG Posterior Cervical Screw System
Regulation
21 CFR 888.3075
Device class
Class II
Review panel
Orthopedic
Applicant
Medos International SARL Chemin-Blanc 38, Lelocle, CH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NKG

Trailing 12 months
5 clearances under product code NKG in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code NKG, trailing twelve months
MonthClearances
November 20251
December 20250
January 20261
February 20260
March 20261
April 20260
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260