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FDA 510(k)

BIOABSORBABLE BANKART TACK

K-Number: K973849 · 1998-01-06

ApplicantHogan & Hartson
Decision Date1998-01-06
Product CodeMAI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BIOABSORBABLE BANKART TACK is the device name listed in this FDA 510(k) record. The listed applicant is Hogan & Hartson. It received FDA 510(k) clearance on 1998-01-06 under 510(k) number K973849. The device is classified under product code MAI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOABSORBABLE BANKART TACK?

BIOABSORBABLE BANKART TACK is a medical device that received FDA 510(k) clearance on 1998-01-06. The listed applicant is Hogan & Hartson. The 510(k) number is K973849.

When did BIOABSORBABLE BANKART TACK receive FDA 510(k) clearance?

BIOABSORBABLE BANKART TACK received FDA 510(k) clearance on 1998-01-06, under 510(k) number K973849.

Who is the listed applicant for BIOABSORBABLE BANKART TACK?

The FDA 510(k) record lists Hogan & Hartson as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOABSORBABLE BANKART TACK?

The FDA product code for BIOABSORBABLE BANKART TACK is MAI.

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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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