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FDA 510(k)

INNOVASIVE 10MM LINX HT LIGAMENT FASTENER

K-Number: K980334 · 1998-04-27

ApplicantInnovasive Devices, Inc.
Decision Date1998-04-27
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INNOVASIVE 10MM LINX HT LIGAMENT FASTENER is the device name listed in this FDA 510(k) record. The listed applicant is Innovasive Devices, Inc.. It received FDA 510(k) clearance on 1998-04-27 under 510(k) number K980334. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INNOVASIVE 10MM LINX HT LIGAMENT FASTENER?

INNOVASIVE 10MM LINX HT LIGAMENT FASTENER is a medical device that received FDA 510(k) clearance on 1998-04-27. The listed applicant is Innovasive Devices, Inc.. The 510(k) number is K980334.

When did INNOVASIVE 10MM LINX HT LIGAMENT FASTENER receive FDA 510(k) clearance?

INNOVASIVE 10MM LINX HT LIGAMENT FASTENER received FDA 510(k) clearance on 1998-04-27, under 510(k) number K980334.

Who is the listed applicant for INNOVASIVE 10MM LINX HT LIGAMENT FASTENER?

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

What is the FDA product code for INNOVASIVE 10MM LINX HT LIGAMENT FASTENER?

The FDA product code for INNOVASIVE 10MM LINX HT LIGAMENT FASTENER is MBI.

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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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