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FDA 510(k)

ACL CLIP-IN PLATE

K-Number: K973874 · 1998-04-24

ApplicantInnovasive Devices, Inc.
Decision Date1998-04-24
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACL CLIP-IN PLATE 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 1998-04-24 under 510(k) number K973874. 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 ACL CLIP-IN PLATE?

ACL CLIP-IN PLATE is a medical device that received FDA 510(k) clearance on 1998-04-24. The listed applicant is Innovasive Devices, Inc.. The 510(k) number is K973874.

When did ACL CLIP-IN PLATE receive FDA 510(k) clearance?

ACL CLIP-IN PLATE received FDA 510(k) clearance on 1998-04-24, under 510(k) number K973874.

Who is the listed applicant for ACL CLIP-IN PLATE?

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 ACL CLIP-IN PLATE?

The FDA product code for ACL CLIP-IN PLATE 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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