FLOWER SMALL AND MEDIUM BONE IMPLANTS
K-Number: K123562 · 2013-03-29
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Device Summary
Frequently Asked Questions
What is the FLOWER SMALL AND MEDIUM BONE IMPLANTS?
FLOWER SMALL AND MEDIUM BONE IMPLANTS is a medical device that received FDA 510(k) clearance on 2013-03-29. The listed applicant is Flower Orthopedics Corporation. The 510(k) number is K123562.
When did FLOWER SMALL AND MEDIUM BONE IMPLANTS receive FDA 510(k) clearance?
FLOWER SMALL AND MEDIUM BONE IMPLANTS received FDA 510(k) clearance on 2013-03-29, under 510(k) number K123562.
Who is the listed applicant for FLOWER SMALL AND MEDIUM BONE IMPLANTS?
The FDA 510(k) record lists Flower Orthopedics Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLOWER SMALL AND MEDIUM BONE IMPLANTS?
The FDA product code for FLOWER SMALL AND MEDIUM BONE IMPLANTS is HRS.
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 Flower Orthopedics Corporation 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: HRS)
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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