OSTEOGRAF/P PERIODONTAL HYDROXYLAPATITE, 40-60— 510(k) K891173

Name: FDA 510(k) clearance K891173
Creator: U.S. Food and Drug Administration
Published: 1989-09-01

Substantially Equivalent

Ceramed Corp.

FDA 510(k) clearance K891173 for OSTEOGRAF/P PERIODONTAL HYDROXYLAPATITE, 40-60, Substantially Equivalent on 1989-09-01. Applicant: Ceramed Corp.. Device class: 2.

Clearance details

Applicant: Ceramed Corp.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 1989-03-06
Decision date: 1989-09-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lakewood, CO, 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 Ceramed Corp.

view all

K962838 — PERMARIDGE SYRINGE1996-08-20
K962786 — OSTEOGRAF STAINLESS STEEL SYRING1996-08-01
K960348 — OSTEOGRAF/N-300 HYDROXYLAPATITE1996-04-22
K960353 — OSTEOGRAF/LD-300 HYDROXYLAPATITE1996-04-18
K960368 — OSTEOGRAFT/N-700 HYDROXYLAPTITE1996-04-18

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