STRYKER TRAUMA PLATING SYSTEM
K-Number: K000636 · 2000-05-11
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Device Summary
Frequently Asked Questions
What is the STRYKER TRAUMA PLATING SYSTEM?
STRYKER TRAUMA PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 2000-05-11. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K000636.
When did STRYKER TRAUMA PLATING SYSTEM receive FDA 510(k) clearance?
STRYKER TRAUMA PLATING SYSTEM received FDA 510(k) clearance on 2000-05-11, under 510(k) number K000636.
Who is the listed applicant for STRYKER TRAUMA PLATING SYSTEM?
The FDA 510(k) record lists Howmedica Osteonics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STRYKER TRAUMA PLATING SYSTEM?
The FDA product code for STRYKER TRAUMA PLATING SYSTEM is HRS.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Howmedica Osteonics Corp. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HRS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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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