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FDA 510(k)

LINK (R) AMERICAN-TYPE BONE STAPLE SYSTEM

K-Number: K873507 · 1987-09-16

ApplicantLink America, Inc.
Decision Date1987-09-16
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LINK (R) AMERICAN-TYPE BONE STAPLE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Link America, Inc.. It received FDA 510(k) clearance on 1987-09-16 under 510(k) number K873507. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINK (R) AMERICAN-TYPE BONE STAPLE SYSTEM?

LINK (R) AMERICAN-TYPE BONE STAPLE SYSTEM is a medical device that received FDA 510(k) clearance on 1987-09-16. The listed applicant is Link America, Inc.. The 510(k) number is K873507.

When did LINK (R) AMERICAN-TYPE BONE STAPLE SYSTEM receive FDA 510(k) clearance?

LINK (R) AMERICAN-TYPE BONE STAPLE SYSTEM received FDA 510(k) clearance on 1987-09-16, under 510(k) number K873507.

Who is the listed applicant for LINK (R) AMERICAN-TYPE BONE STAPLE SYSTEM?

The FDA 510(k) record lists Link America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LINK (R) AMERICAN-TYPE BONE STAPLE SYSTEM?

The FDA product code for LINK (R) AMERICAN-TYPE BONE STAPLE SYSTEM is JDR.

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Other records listing Link America, Inc. as applicant

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Related Devices (Code: JDR)

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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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