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FDA 510(k)

MINVASIVE SUTURE BONE FASTENER

K-Number: K924034 · 1993-08-24

ApplicantInnovasive Devices, Inc.
Decision Date1993-08-24
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MINVASIVE SUTURE BONE 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 1993-08-24 under 510(k) number K924034. 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 MINVASIVE SUTURE BONE FASTENER?

MINVASIVE SUTURE BONE FASTENER is a medical device that received FDA 510(k) clearance on 1993-08-24. The listed applicant is Innovasive Devices, Inc.. The 510(k) number is K924034.

When did MINVASIVE SUTURE BONE FASTENER receive FDA 510(k) clearance?

MINVASIVE SUTURE BONE FASTENER received FDA 510(k) clearance on 1993-08-24, under 510(k) number K924034.

Who is the listed applicant for MINVASIVE SUTURE BONE 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 MINVASIVE SUTURE BONE FASTENER?

The FDA product code for MINVASIVE SUTURE BONE FASTENER is JDR.

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Other records listing Innovasive Devices, Inc. as applicant

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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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