ORTHOSORB LS— 510(k) K140625

Substantially Equivalent

Biomet, Inc.

FDA 510(k) clearance K140625 for ORTHOSORB LS, Substantially Equivalent on 2014-04-18. Applicant: Biomet, Inc.. Device class: 2.

Clearance details

Applicant: Biomet, Inc.
Product code: Code OVZ
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 2014-03-11
Decision date: 2014-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warsaw, IN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code OVZ

K111077 — ORTHOSORB RESORBABLE PINS2011-07-12
K901456 — ORTHOSORB(R) ABSORBABLE PIN1990-08-15

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