ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202
K-Number: K870329 · 1987-02-13
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Device Summary
Frequently Asked Questions
What is the ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202?
ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202 is a medical device that received FDA 510(k) clearance on 1987-02-13. The listed applicant is Biodynamic Technologies, Inc.. The 510(k) number is K870329.
When did ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202 receive FDA 510(k) clearance?
ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202 received FDA 510(k) clearance on 1987-02-13, under 510(k) number K870329.
Who is the listed applicant for ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202?
The FDA 510(k) record lists Biodynamic Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202?
The FDA product code for ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202 is HTR.
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 Biodynamic Technologies, 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: HTR)
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.
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