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)

ANATOMIC TOTAL KNEE PROSTHESIS

K-Number: K000978 · 2000-06-22

ApplicantBiomet, Inc.
Decision Date2000-06-22
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ANATOMIC TOTAL KNEE PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2000-06-22 under 510(k) number K000978. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANATOMIC TOTAL KNEE PROSTHESIS?

ANATOMIC TOTAL KNEE PROSTHESIS is a medical device that received FDA 510(k) clearance on 2000-06-22. The listed applicant is Biomet, Inc.. The 510(k) number is K000978.

When did ANATOMIC TOTAL KNEE PROSTHESIS receive FDA 510(k) clearance?

ANATOMIC TOTAL KNEE PROSTHESIS received FDA 510(k) clearance on 2000-06-22, under 510(k) number K000978.

Who is the listed applicant for ANATOMIC TOTAL KNEE PROSTHESIS?

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

What is the FDA product code for ANATOMIC TOTAL KNEE PROSTHESIS?

The FDA product code for ANATOMIC TOTAL KNEE PROSTHESIS is JWH.

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 Biomet, Inc. 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.

View all 418 devices →

Related Devices (Code: JWH)

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.

↑