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FDA 510(k)

RESORBABLE SOFT TISSUE ATTACHMENT DEVICE

K-Number: K950275 · 1995-11-07

ApplicantZimmer, Inc.
Decision Date1995-11-07
Product CodeMAI
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

RESORBABLE SOFT TISSUE ATTACHMENT DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1995-11-07 under 510(k) number K950275. The device is classified under product code MAI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the RESORBABLE SOFT TISSUE ATTACHMENT DEVICE?

RESORBABLE SOFT TISSUE ATTACHMENT DEVICE is a medical device that received FDA 510(k) clearance on 1995-11-07. The listed applicant is Zimmer, Inc.. The 510(k) number is K950275.

When did RESORBABLE SOFT TISSUE ATTACHMENT DEVICE receive FDA 510(k) clearance?

RESORBABLE SOFT TISSUE ATTACHMENT DEVICE received FDA 510(k) clearance on 1995-11-07, under 510(k) number K950275.

Who is the listed applicant for RESORBABLE SOFT TISSUE ATTACHMENT DEVICE?

The FDA 510(k) record lists Zimmer, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RESORBABLE SOFT TISSUE ATTACHMENT DEVICE?

The FDA product code for RESORBABLE SOFT TISSUE ATTACHMENT DEVICE is MAI.

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Other records listing Zimmer, 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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