FDA 510(k)

Wishbone HA

K-Number: K211551 · 2021-08-20

Decision Date2021-08-20

Product CodeNPM

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

Wishbone HA is the device name listed in this FDA 510(k) record. The listed applicant is Wishbone SA. It received FDA 510(k) clearance on 2021-08-20 under 510(k) number K211551. The device is classified under product code NPM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Wishbone HA?

Wishbone HA is a medical device that received FDA 510(k) clearance on 2021-08-20. The listed applicant is Wishbone SA. The 510(k) number is K211551.

When did Wishbone HA receive FDA 510(k) clearance?

Wishbone HA received FDA 510(k) clearance on 2021-08-20, under 510(k) number K211551.

Who is the listed applicant for Wishbone HA?

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

What is the FDA product code for Wishbone HA?

The FDA product code for Wishbone HA is NPM.

Related Devices (Code: NPM)

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.

K253723BOSSMedpark Co., Ltd.K251786Geistlich Bio-Oss®; Geistlich Bio-Oss Pen®Geistlich Pharma AG K251613SwissGraft XGeistlich Pharma AG K242510Geistlich Bio-Flow®Geistlich Pharma AG K240133Xenograft Bovine Bone ParticulateCollagen Solutions, LLC K230305THE Graft CollagenPurgo Biologics, Inc.

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.