IMPLANTECH LATERAL MANDIBULAR BAR IMPLANT— 510(k) K942421

Name: FDA 510(k) clearance K942421
Creator: U.S. Food and Drug Administration
Published: 1994-08-08

Substantially Equivalent

King & Spalding

FDA 510(k) clearance K942421 for IMPLANTECH LATERAL MANDIBULAR BAR IMPLANT, Substantially Equivalent on 1994-08-08. Applicant: King & Spalding. Device class: 2.

Clearance details

Applicant: King & Spalding
Product code: Code LZK
Device class: Class 2
Regulation: 21 CFR 878.3550
Advisory panel: General, Plastic Surgery
Date received: 1994-05-20
Decision date: 1994-08-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LZK

view all

K021419 — AART MALAR IMPLANT2002-07-02
K002886 — IMPLANTECH COMPOSITE FACIAL IMPLANTS (MALAR, CHIN, AND NASAL)2000-11-24
K992240 — PILLAR MALAR IMPLANT1999-11-22
K983756 — SURGIFORM ANATOMICAL MALAR1998-11-20
K982763 — SEARE BIOMEDICAL MALAR IMPLANTS1998-09-30

More clearances from King & Spalding

view all

K942422 — PANASONIC WRIST BLOOD PRESSURE METER1995-02-15
K942423 — NAIS WRIST BLOOD PRESSURE METER1995-02-15
K945998 — CHIN IMPLANT STYLE I1995-02-07
K944408 — IMPLANTECH MEDICAL GRADE SILICONE SHEETING1994-11-09
K942420 — IMPLANTECH MIDFACE-SUBMALAR LE FORT IMPLANT1994-08-08

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