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FDA 510(k)

PRO Plating System, Stryker Trauma Pelvic Set (Matta)

K-Number: K223772 · 2023-04-07

ApplicantStryker GmbH
Decision Date2023-04-07
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PRO Plating System, Stryker Trauma Pelvic Set (Matta) is a medical device manufactured by Stryker GmbH. It received FDA 510(k) clearance on 2023-04-07 under approval number K223772. 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 PRO Plating System, Stryker Trauma Pelvic Set (Matta)?

PRO Plating System, Stryker Trauma Pelvic Set (Matta) is a medical device that received FDA 510(k) clearance on 2023-04-07. It is manufactured by Stryker GmbH. The 510(k) number is K223772.

When was PRO Plating System, Stryker Trauma Pelvic Set (Matta) approved by the FDA?

PRO Plating System, Stryker Trauma Pelvic Set (Matta) received FDA 510(k) clearance on 2023-04-07, under approval number K223772.

What company makes PRO Plating System, Stryker Trauma Pelvic Set (Matta)?

PRO Plating System, Stryker Trauma Pelvic Set (Matta) is manufactured by Stryker GmbH.

What is the FDA product code for PRO Plating System, Stryker Trauma Pelvic Set (Matta)?

The FDA product code for PRO Plating System, Stryker Trauma Pelvic Set (Matta) is HRS.

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Related PubMed Literature

PMID: 42056377 Signal detection of adverse events in medical devices using natural language processing: a case study in pelvic mesh. Scientific reports (2026)

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Related Devices (Code: HRS)

K163086VLP MINI-MOD 2.0mm Column PlatesSmith & Nephew, Inc. K162829Medline UNITE® Ankle Fracture Plating SystemMedline Industries, Inc. K162974Biomet Microfixation RibFix Blu Thoracic Fixation SystemBiomet Microfixation K163007Biomet Microfixation SternaLock 360 Sternal Closure SystemBiomet Microfixation K161696aap LOQTEQ® Distal Lateral Humerus Plate 2.7/3.5Aap Implantate AG K161747LOQTEQ® VA Distal Tibia Plate System: LOQTEQ® VA Distal Medial Tibia Plate 3.5; LOQTEQ® VA Distal Anterolateral Tibia Plate 3.5; LOQTEQ® VA Distal Fibula Plate 2.7/3.5Aap Implantate AG

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.

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