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FDA 510(k)

RC TACK

K-Number: K992377 · 1999-10-08

ApplicantInnovasive Devices, Inc.
Decision Date1999-10-08
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RC TACK 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 1999-10-08 under 510(k) number K992377. 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 TACK?

RC TACK is a medical device that received FDA 510(k) clearance on 1999-10-08. The listed applicant is Innovasive Devices, Inc.. The 510(k) number is K992377.

When did RC TACK receive FDA 510(k) clearance?

RC TACK received FDA 510(k) clearance on 1999-10-08, under 510(k) number K992377.

Who is the listed applicant for RC TACK?

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 TACK?

The FDA product code for RC TACK is MBI.

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.

K994269TITAN RC TACKK993975ABSOLUTE ABSORBABLE INTERFERENCE SCREWK992458RC MULTISUTURE BONE ANCHOR, MODEL 4453/4454K990454BIO-INTERFERENCE SCREWK984490SUTURELESS ANCHORK983560INNOVASIVE DEVICES INTRATUNNEL TIBIAL FIXATION FASTENER

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Related Devices (Code: MBI)

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.

K261869Integrity Retractable Implant Inserter (6000127)Anika Therapeutics, Inc.K262809ArthroTAK Tendon Anchor KitArthroTAK, LLCK253065Aevumed SUPERCYNCH™ Button SystemAevumed, Inc.K262677Iconix Knotless TRiverpoint MedicalK262047Grappler Suture Anchor SystemParagon 28, Inc.K262369AIR+ All-Inside Meniscal Repair Device, Curved Up;AIR+ All-Inside Meniscal Repair Device, Curved DownStryker Endoscopy

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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