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FDA 510(k)

NEER-III OSTEOARTHRITIS GLENOID RESURFACE PROSTHE.

K-Number: K873620 · 1987-10-15

ApplicantKirschner Medical Corp.
Decision Date1987-10-15
Product CodeKWT
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

NEER-III OSTEOARTHRITIS GLENOID RESURFACE PROSTHE. is the device name listed in this FDA 510(k) record. The listed applicant is Kirschner Medical Corp.. It received FDA 510(k) clearance on 1987-10-15 under 510(k) number K873620. The device is classified under product code KWT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the NEER-III OSTEOARTHRITIS GLENOID RESURFACE PROSTHE.?

NEER-III OSTEOARTHRITIS GLENOID RESURFACE PROSTHE. is a medical device that received FDA 510(k) clearance on 1987-10-15. The listed applicant is Kirschner Medical Corp.. The 510(k) number is K873620.

When did NEER-III OSTEOARTHRITIS GLENOID RESURFACE PROSTHE. receive FDA 510(k) clearance?

NEER-III OSTEOARTHRITIS GLENOID RESURFACE PROSTHE. received FDA 510(k) clearance on 1987-10-15, under 510(k) number K873620.

Who is the listed applicant for NEER-III OSTEOARTHRITIS GLENOID RESURFACE PROSTHE.?

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

What is the FDA product code for NEER-III OSTEOARTHRITIS GLENOID RESURFACE PROSTHE.?

The FDA product code for NEER-III OSTEOARTHRITIS GLENOID RESURFACE PROSTHE. is KWT.

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Other records listing Kirschner Medical 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.

K940537KIRSCHNER(R) MODULAR II-C(TM) TOTAL SHOULDER SYSTEMK936274KIRSCHNER PERFORMANCE POSTERIOR STABILIZED TOTAL KNEE SYSTEMK942891SUMMIT TOTAL HIP SYSTEMK941486INTEGRITY TOTAL HIP SYSTEM, NON-POROUSK933843LINE EXTENSION FOR KIRSCHNER PERFORMANCE TOTAL KNEE SYSTEM, POROUS COATEDK935951KIRSCHNER C-2 OSTEOCAP TOTAL HIP SYSTEM

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Related Devices (Code: KWT)

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.

K262173N22 Offset Humeral HeadShoulder Innovations, Inc.K250713Equinoxe® Humeral Reconstruction Prosthesis; Equinoxe® Stemless Shoulder ImplantsExactech, Inc.K251686Tornier Humeral Reconstruction System Max (Tornier HRS Max)Tornier, Inc.K241944AGILON® XO Shoulder Replacement SystemImplantcast GmbHK241817InSet Total Shoulder SystemShoulder Innovations, Inc.K231657AGILON® XO Shoulder Replacement SystemImplantcast GmbH

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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