Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CARPAL ENGAGING WRIST FUSION PLATE

K-Number: K974030 · 1998-01-21

ApplicantTerray Corp.
Decision Date1998-01-21
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CARPAL ENGAGING WRIST FUSION PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Terray Corp.. It received FDA 510(k) clearance on 1998-01-21 under 510(k) number K974030. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARPAL ENGAGING WRIST FUSION PLATE?

CARPAL ENGAGING WRIST FUSION PLATE is a medical device that received FDA 510(k) clearance on 1998-01-21. The listed applicant is Terray Corp.. The 510(k) number is K974030.

When did CARPAL ENGAGING WRIST FUSION PLATE receive FDA 510(k) clearance?

CARPAL ENGAGING WRIST FUSION PLATE received FDA 510(k) clearance on 1998-01-21, under 510(k) number K974030.

Who is the listed applicant for CARPAL ENGAGING WRIST FUSION PLATE?

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

What is the FDA product code for CARPAL ENGAGING WRIST FUSION PLATE?

The FDA product code for CARPAL ENGAGING WRIST FUSION PLATE is HRS.

Related Clinical Trials

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.

Other records listing Terray Corp. as applicant

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.

Related Devices (Code: HRS)

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.

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.

↑