LORENZ STENT— 510(k) K896667

Substantially Equivalent

Walter Lorenz Surgical, Inc.

FDA 510(k) clearance K896667 for LORENZ STENT, Substantially Equivalent on 1990-02-22. Applicant: Walter Lorenz Surgical, Inc.. Device class: 2.

Clearance details

Applicant: Walter Lorenz Surgical, Inc.
Product code: Code FWN
Device class: Class 2
Regulation: 21 CFR 874.3620
Advisory panel: Ear, Nose, Throat
Date received: 1989-11-27
Decision date: 1990-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Walter Lorenz Surgical, Inc.

K063386 — LORENZ ORTHODONTIC ANCHORAGE SYSTEM2007-02-09
K063052 — LORENZ TITANIUM FRACTURE / RECONSTRUCTION DEVICES AND PRE-BENT PLATES2007-01-12
K063506 — LORENZ STERNAL CLOSURE SYSTEM2006-12-18
K062842 — TWIST DRILL2006-12-04
K061384 — LORENZ PECTUS SUPPORT BAR, TITANIUM; LORENZ PECTUS SUPPORT BAR STABILIZER, TITANIUM2006-06-06

Data sourced from openFDA. This site is unofficial and independent of the FDA.