STRYKER INJECTABLE CEMENT— 510(k) K060750

Substantially Equivalent

Stryker Cmf

FDA 510(k) clearance K060750 for STRYKER INJECTABLE CEMENT, Substantially Equivalent on 2006-04-19. Applicant: Stryker Cmf. Device class: 2.

Clearance details

Applicant: Stryker Cmf
Product code: Code NEA
Device class: Class 2
Regulation: 21 CFR 872.3275
Advisory panel: Dental
Date received: 2006-03-21
Decision date: 2006-04-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code NEA

K140644 — PROCEM2014-06-19
K080032 — ENVOYCEM, MODEL 16402008-02-28
K042516 — OTOMIMIX2004-11-08
K011338 — OTO-CEM2001-09-13
K003567 — SERENOCEM, MODEL BC 0102001-02-12

More clearances from Stryker Cmf

K071628 — STRYKER EXTERNAL FIXATION SYSTEM2007-08-10

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