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FDA 510(k)

DAVIS & GECK VALTRAC(R) BIOFRAG ANASTOMOSIS RING

K-Number: K913411 · 1991-09-06

ApplicantDavis & Geck, Inc.
Decision Date1991-09-06
Product CodeGDW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DAVIS & GECK VALTRAC(R) BIOFRAG ANASTOMOSIS RING is the device name listed in this FDA 510(k) record. The listed applicant is Davis & Geck, Inc.. It received FDA 510(k) clearance on 1991-09-06 under 510(k) number K913411. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAVIS & GECK VALTRAC(R) BIOFRAG ANASTOMOSIS RING?

DAVIS & GECK VALTRAC(R) BIOFRAG ANASTOMOSIS RING is a medical device that received FDA 510(k) clearance on 1991-09-06. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K913411.

When did DAVIS & GECK VALTRAC(R) BIOFRAG ANASTOMOSIS RING receive FDA 510(k) clearance?

DAVIS & GECK VALTRAC(R) BIOFRAG ANASTOMOSIS RING received FDA 510(k) clearance on 1991-09-06, under 510(k) number K913411.

Who is the listed applicant for DAVIS & GECK VALTRAC(R) BIOFRAG ANASTOMOSIS RING?

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

What is the FDA product code for DAVIS & GECK VALTRAC(R) BIOFRAG ANASTOMOSIS RING?

The FDA product code for DAVIS & GECK VALTRAC(R) BIOFRAG ANASTOMOSIS RING is GDW.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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