PERMAMESH HYDROXYLAPATITE MATRIX— 510(k) K960362

Substantially Equivalent

Ceramed Corp.

FDA 510(k) clearance K960362 for PERMAMESH HYDROXYLAPATITE MATRIX, Substantially Equivalent on 1996-03-20. Applicant: Ceramed Corp.. Device class: 2.

Clearance details

Applicant: Ceramed Corp.
Product code: Code LZK
Device class: Class 2
Regulation: 21 CFR 878.3550
Advisory panel: General, Plastic Surgery
Date received: 1996-01-25
Decision date: 1996-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lakewood, CO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LZK

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 Ceramed Corp.

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.