Z2017, BEA/CNA 5%SB BIPLATE
K-Number: K870340 · 1987-02-13
Advertisement
Device Summary
Frequently Asked Questions
What is the Z2017, BEA/CNA 5%SB BIPLATE?
Z2017, BEA/CNA 5%SB BIPLATE is a medical device that received FDA 510(k) clearance on 1987-02-13. The listed applicant is Lakewood Biochemical Co., Inc.. The 510(k) number is K870340.
When did Z2017, BEA/CNA 5%SB BIPLATE receive FDA 510(k) clearance?
Z2017, BEA/CNA 5%SB BIPLATE received FDA 510(k) clearance on 1987-02-13, under 510(k) number K870340.
Who is the listed applicant for Z2017, BEA/CNA 5%SB BIPLATE?
The FDA 510(k) record lists Lakewood Biochemical Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Z2017, BEA/CNA 5%SB BIPLATE?
The FDA product code for Z2017, BEA/CNA 5%SB BIPLATE is JSI.
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 Lakewood Biochemical Co., 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.
Related Devices (Code: JSI)
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.
Advertisement