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FDA 510(k)

RC MULTISUTURE BONE ANCHOR, MODEL 4453/4454

K-Number: K992458 · 1999-10-14

ApplicantInnovasive Devices, Inc.
Decision Date1999-10-14
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RC MULTISUTURE BONE ANCHOR, MODEL 4453/4454 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 1999-10-14 under 510(k) number K992458. 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 RC MULTISUTURE BONE ANCHOR, MODEL 4453/4454?

RC MULTISUTURE BONE ANCHOR, MODEL 4453/4454 is a medical device that received FDA 510(k) clearance on 1999-10-14. The listed applicant is Innovasive Devices, Inc.. The 510(k) number is K992458.

When did RC MULTISUTURE BONE ANCHOR, MODEL 4453/4454 receive FDA 510(k) clearance?

RC MULTISUTURE BONE ANCHOR, MODEL 4453/4454 received FDA 510(k) clearance on 1999-10-14, under 510(k) number K992458.

Who is the listed applicant for RC MULTISUTURE BONE ANCHOR, MODEL 4453/4454?

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 RC MULTISUTURE BONE ANCHOR, MODEL 4453/4454?

The FDA product code for RC MULTISUTURE BONE ANCHOR, MODEL 4453/4454 is MBI.

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Other records listing Innovasive Devices, Inc. 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.

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Related Devices (Code: 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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