BONE STAPLING FIXATION SYS
K-Number: K840566 · 1984-11-23
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Device Summary
Frequently Asked Questions
What is the BONE STAPLING FIXATION SYS?
BONE STAPLING FIXATION SYS is a medical device that received FDA 510(k) clearance on 1984-11-23. The listed applicant is 3M Company. The 510(k) number is K840566.
When did BONE STAPLING FIXATION SYS receive FDA 510(k) clearance?
BONE STAPLING FIXATION SYS received FDA 510(k) clearance on 1984-11-23, under 510(k) number K840566.
Who is the listed applicant for BONE STAPLING FIXATION SYS?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BONE STAPLING FIXATION SYS?
The FDA product code for BONE STAPLING FIXATION SYS is JDR.
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 3M Company 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: JDR)
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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