PYROLITE CARBON ALVEOLAR MAINTEN IMPLANT— 510(k) K791416

Name: FDA 510(k) clearance K791416
Creator: U.S. Food and Drug Administration
Published: 1979-10-09

Substantially Equivalent

Carbomedics, Inc.

FDA 510(k) clearance K791416 for PYROLITE CARBON ALVEOLAR MAINTEN IMPLANT, Substantially Equivalent on 1979-10-09. Applicant: Carbomedics, Inc.. Device class: 2.

Clearance details

Applicant: Carbomedics, Inc.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 1979-07-26
Decision date: 1979-10-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LYC

view all

K253317 — Cytrans Elashield2026-07-06
K253883 — Bonalive Maxillofacial2026-05-14
K251818 — BONTREE PLUS2026-03-06
K244006 — FG Bone Graft M2025-09-17
K243745 — FG Bone Graft B2025-08-29

More clearances from Carbomedics, Inc.

view all

K970375 — ANNULOFLO SYSTEM1997-07-25
K964665 — VASCUTEK GELWEAVE VASCULAR GRAFT (BIFURCATED CONFIGURATION)1997-02-19
K962154 — CARBOMEDICS HANDLE1996-08-27
K960923 — CARBOMEDICS MITRAL ROTATOR1996-04-29
K960706 — VASCUTEK VASCUSOFT PLUS VASCULAR GRAFT1996-04-25

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