FIXATION STAPLE KIT - DLIDE HAMMER
K-Number: K834515 · 1984-04-23
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Device Summary
Frequently Asked Questions
What is the FIXATION STAPLE KIT - DLIDE HAMMER?
FIXATION STAPLE KIT - DLIDE HAMMER is a medical device that received FDA 510(k) clearance on 1984-04-23. The listed applicant is Stryker Corp.. The 510(k) number is K834515.
When did FIXATION STAPLE KIT - DLIDE HAMMER receive FDA 510(k) clearance?
FIXATION STAPLE KIT - DLIDE HAMMER received FDA 510(k) clearance on 1984-04-23, under 510(k) number K834515.
Who is the listed applicant for FIXATION STAPLE KIT - DLIDE HAMMER?
The FDA 510(k) record lists Stryker Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FIXATION STAPLE KIT - DLIDE HAMMER?
The FDA product code for FIXATION STAPLE KIT - DLIDE HAMMER is HXJ.
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 Stryker 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: HXJ)
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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