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)

2.5 MM LACTOSORB SCREWS

K-Number: K981666 · 1998-11-03

ApplicantBiomet, Inc.
Decision Date1998-11-03
Product CodeDZL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

2.5 MM LACTOSORB SCREWS is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1998-11-03 under 510(k) number K981666. The device is classified under product code DZL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 2.5 MM LACTOSORB SCREWS?

2.5 MM LACTOSORB SCREWS is a medical device that received FDA 510(k) clearance on 1998-11-03. The listed applicant is Biomet, Inc.. The 510(k) number is K981666.

When did 2.5 MM LACTOSORB SCREWS receive FDA 510(k) clearance?

2.5 MM LACTOSORB SCREWS received FDA 510(k) clearance on 1998-11-03, under 510(k) number K981666.

Who is the listed applicant for 2.5 MM LACTOSORB SCREWS?

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 2.5 MM LACTOSORB SCREWS?

The FDA product code for 2.5 MM LACTOSORB SCREWS is DZL.

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: DZL)

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.

↑