ABG II MONOLITHIC HIP STEM— 510(k) K110807

Substantially Equivalent

Stryker Corp.

FDA 510(k) clearance K110807 for ABG II MONOLITHIC HIP STEM, Substantially Equivalent on 2011-05-25. Applicant: Stryker Corp.. Device class: 2.

Clearance details

Applicant: Stryker Corp.
Product code: Code MAY
Device class: Class 2
Regulation: 21 CFR 888.3353
Advisory panel: Orthopedic
Date received: 2011-03-23
Decision date: 2011-05-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mahwah, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MAY

K123604 — ABG III MONOLITHIC HIP STEM2013-08-16
K090103 — 100KGY E-POLY ACETABULAR LINERS- ADDITIONAL PROFILES: +3 MAXROM AND +3 HI-WALL2009-02-11
K051844 — EQUATOR PLUS ACETABULAR CUP SYSTEM2005-10-07

More clearances from Stryker Corp.

K230045 — HipCheck2023-09-29
K191259 — Stryker CrossFlow Integrated Arthroscopy Pump2019-07-12
K182359 — HipCheck2018-12-13
K143399 — Stryker Footed Attachments and Cutting Accessories2015-05-08
K143320 — Stryker Elite Attachments, Stryker Heavy Duty (HD) Attachments2015-04-23

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