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FDA 510(k)

NEER-III SOLID KEEL GLENOID RESURFACING PROSTHESIS

K-Number: K873621 · 1987-10-15

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

Device Summary

NEER-III SOLID KEEL GLENOID RESURFACING PROSTHESIS 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 K873621. 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 SOLID KEEL GLENOID RESURFACING PROSTHESIS?

NEER-III SOLID KEEL GLENOID RESURFACING PROSTHESIS 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 K873621.

When did NEER-III SOLID KEEL GLENOID RESURFACING PROSTHESIS receive FDA 510(k) clearance?

NEER-III SOLID KEEL GLENOID RESURFACING PROSTHESIS received FDA 510(k) clearance on 1987-10-15, under 510(k) number K873621.

Who is the listed applicant for NEER-III SOLID KEEL GLENOID RESURFACING PROSTHESIS?

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 SOLID KEEL GLENOID RESURFACING PROSTHESIS?

The FDA product code for NEER-III SOLID KEEL GLENOID RESURFACING PROSTHESIS is KWT.

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Other records listing Kirschner Medical Corp. as applicant

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Related Devices (Code: KWT)

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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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