Cleared Traditional

K101458 - LINA XCISE MODEL MOR-1515
(FDA 510(k) Clearance)

Mar 2011
Decision
289d
Days
Class 2
Risk

K101458 is an FDA 510(k) clearance for the LINA XCISE MODEL MOR-1515. This device is classified as a Laparoscope, Gynecologic (and Accessories) (Class II - Special Controls, product code HET).

Submitted by Lina Medical Aps (Chapel Hill, US). The FDA issued a Cleared decision on March 11, 2011, 289 days after receiving the submission on May 26, 2010.

This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.1720.

Submission Details

510(k) Number K101458 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 26, 2010
Decision Date March 11, 2011
Days to Decision 289 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF

Device Classification

Product Code HET — Laparoscope, Gynecologic (and Accessories)
Device Class Class II - Special Controls
CFR Regulation 21 CFR 884.1720

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