FDA 510(k)

COVENTRY STAPLE

K-Number: K761064 · 1976-12-30

Decision Date1976-12-30

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

COVENTRY STAPLE is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1976-12-30 under 510(k) number K761064. 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 COVENTRY STAPLE?

COVENTRY STAPLE is a medical device that received FDA 510(k) clearance on 1976-12-30. The listed applicant is Depuy, Inc.. The 510(k) number is K761064.

When did COVENTRY STAPLE receive FDA 510(k) clearance?

COVENTRY STAPLE received FDA 510(k) clearance on 1976-12-30, under 510(k) number K761064.

Who is the listed applicant for COVENTRY STAPLE?

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

What is the FDA product code for COVENTRY STAPLE?

The FDA product code for COVENTRY STAPLE is GDW.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Depuy, Inc. as applicant

K043058PINNACLE CONSTRAINED ACETABULAR LINERS K042664LPS UPPER EXTREMITY K041085LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARY K033959LPS K040544DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044 TO -062 AND 1599-21-044 TO -062 K021478DELTA SHOULDER

View all 303 devices →

Related Devices (Code: GDW)

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.