CRANIOFACIAL CALCIUM PHOSPHATE CERAMIC BONE FILLER— 510(k) K990290

Name: FDA 510(k) clearance K990290
Creator: U.S. Food and Drug Administration
Published: 1999-11-18

Substantially Equivalent

Biomet, Inc.

FDA 510(k) clearance K990290 for CRANIOFACIAL CALCIUM PHOSPHATE CERAMIC BONE FILLER, Substantially Equivalent on 1999-11-18. Applicant: Biomet, Inc.. Device class: 2.

Clearance details

Applicant: Biomet, Inc.
Product code: Code GXP
Device class: Class 2
Regulation: 21 CFR 882.5300
Advisory panel: Neurology
Date received: 1999-01-29
Decision date: 1999-11-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warsaw, IN, US

Download summary PDF View on FDA.gov ↗

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