510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
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K092239Substantially Equivalent

Rosa Surgical Device, Model Rosa 1.1

MedTech LLC, Montpellier, FR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K092239 is the FDA 510(k) clearance record for ROSA SURGICAL DEVICE, MODEL ROSA 1.1, a class II device, cleared for Medtech S.A on under FDA product code HAW (Neurological Stereotaxic Instrument). FDA records list 9 510(k) clearances for Medtech S.A, from to . As of , FDA records show 9 recalls naming K092239.

Clearance record

Decision date
Received
(117 days to decision)
Product code
HAW Neurological Stereotaxic Instrument
Regulation
21 CFR 882.4560
Device class
Class II
Review panel
Neurology
Applicant
Medtech S.A 1006 Rue De La Croix Verte, Montpellier, FR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HAW

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