GENERATION 5 LINKOW BLADE IMPLANTS— 510(k) K822969

Name: FDA 510(k) clearance K822969
Creator: U.S. Food and Drug Administration
Published: 1982-11-04

Substantially Equivalent

Leonard P. Linkow, D.D.L.

FDA 510(k) clearance K822969 for GENERATION 5 LINKOW BLADE IMPLANTS, Substantially Equivalent on 1982-11-04. Applicant: Leonard P. Linkow, D.D.L.. Device class: 2.

Clearance details

Applicant: Leonard P. Linkow, D.D.L.
Product code: Code NRQ
Device class: Class 2
Regulation: 21 CFR 872.3640
Advisory panel: Dental
Date received: 1982-10-08
Decision date: 1982-11-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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K791366 — ORATRONICS ENDOSSEOUS FRAME ASSEMBLY1979-10-09
K791204 — MITER ENDOSTEAL BLADE IMPLANT1979-09-28

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