Anchorage Bone Plating System
K-Number: K172148 · 2018-03-19
ApplicantStryker GmbH
Decision Date2018-03-19
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Anchorage Bone Plating System is a medical device manufactured by Stryker GmbH. It received FDA 510(k) clearance on 2018-03-19 under approval number K172148. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Anchorage Bone Plating System?
Anchorage Bone Plating System is a medical device that received FDA 510(k) clearance on 2018-03-19. It is manufactured by Stryker GmbH. The 510(k) number is K172148.
When was Anchorage Bone Plating System approved by the FDA?
Anchorage Bone Plating System received FDA 510(k) clearance on 2018-03-19, under approval number K172148.
What company makes Anchorage Bone Plating System?
Anchorage Bone Plating System is manufactured by Stryker GmbH.
What is the FDA product code for Anchorage Bone Plating System?
The FDA product code for Anchorage Bone Plating System is HRS.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.