510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K141835Substantially Equivalent

Romeo Posterior Osteosynthesis System Prebent Cross-Connectors; Prebent Rods

Spineart SA, Geneva, CH / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K141835 is the FDA 510(k) clearance record for ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM PREBENT CROSS-CONNECTORS; PREBENT RODS, a class II device, cleared for Spineart on under FDA product code MNI (Orthosis, Spinal Pedicle Fixation). FDA records list 57 510(k) clearances for Spineart, from to . As of , FDA records show no recalls naming K141835.

Clearance record

Decision date
Received
(65 days to decision)
Product code
MNI Orthosis, Spinal Pedicle Fixation
Regulation
21 CFR 888.3070
Device class
Class II
Review panel
Orthopedic
Applicant
Spineart 20 Rte. De Pre-Bois Cp1813, Geneva, CH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MNI

Trailing 12 months

FDA records hold no clearances under product code MNI in the trailing twelve months.

FDA records show no clearances under product code MNI in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MNI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260