SINGLE/MULTIPLE COMPONENT METALLIC BONE FIXATION
K-Number: K860600 · 1986-03-13
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Device Summary
Frequently Asked Questions
What is the SINGLE/MULTIPLE COMPONENT METALLIC BONE FIXATION?
SINGLE/MULTIPLE COMPONENT METALLIC BONE FIXATION is a medical device that received FDA 510(k) clearance on 1986-03-13. The listed applicant is 3M Company. The 510(k) number is K860600.
When did SINGLE/MULTIPLE COMPONENT METALLIC BONE FIXATION receive FDA 510(k) clearance?
SINGLE/MULTIPLE COMPONENT METALLIC BONE FIXATION received FDA 510(k) clearance on 1986-03-13, under 510(k) number K860600.
Who is the listed applicant for SINGLE/MULTIPLE COMPONENT METALLIC BONE FIXATION?
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 SINGLE/MULTIPLE COMPONENT METALLIC BONE FIXATION?
The FDA product code for SINGLE/MULTIPLE COMPONENT METALLIC BONE FIXATION 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 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: 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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