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FDA 510(k)

STAINLESS 22-13-5 SUTURE WIRE

K-Number: K873645 · 1987-11-17

ApplicantZimmer, Inc.
Decision Date1987-11-17
Product CodeGAQ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STAINLESS 22-13-5 SUTURE WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1987-11-17 under 510(k) number K873645. The device is classified under product code GAQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAINLESS 22-13-5 SUTURE WIRE?

STAINLESS 22-13-5 SUTURE WIRE is a medical device that received FDA 510(k) clearance on 1987-11-17. The listed applicant is Zimmer, Inc.. The 510(k) number is K873645.

When did STAINLESS 22-13-5 SUTURE WIRE receive FDA 510(k) clearance?

STAINLESS 22-13-5 SUTURE WIRE received FDA 510(k) clearance on 1987-11-17, under 510(k) number K873645.

Who is the listed applicant for STAINLESS 22-13-5 SUTURE WIRE?

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 STAINLESS 22-13-5 SUTURE WIRE?

The FDA product code for STAINLESS 22-13-5 SUTURE WIRE is GAQ.

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Related Devices (Code: GAQ)

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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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