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)

ORTHOPAEDIC TABLE 1420

K-Number: K873273 · 1987-09-17

Decision Date1987-09-17
Product CodeJEB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ORTHOPAEDIC TABLE 1420 is the device name listed in this FDA 510(k) record. The listed applicant is Stierlen-Maquet AG. It received FDA 510(k) clearance on 1987-09-17 under 510(k) number K873273. The device is classified under product code JEB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOPAEDIC TABLE 1420?

ORTHOPAEDIC TABLE 1420 is a medical device that received FDA 510(k) clearance on 1987-09-17. The listed applicant is Stierlen-Maquet AG. The 510(k) number is K873273.

When did ORTHOPAEDIC TABLE 1420 receive FDA 510(k) clearance?

ORTHOPAEDIC TABLE 1420 received FDA 510(k) clearance on 1987-09-17, under 510(k) number K873273.

Who is the listed applicant for ORTHOPAEDIC TABLE 1420?

The FDA 510(k) record lists Stierlen-Maquet AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ORTHOPAEDIC TABLE 1420?

The FDA product code for ORTHOPAEDIC TABLE 1420 is JEB.

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 Stierlen-Maquet AG 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 10 devices →

Related Devices (Code: JEB)

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.

↑