SYNTHES ZERO-P
K-Number: K072981 · 2008-02-11
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Device Summary
Frequently Asked Questions
What is the SYNTHES ZERO-P?
SYNTHES ZERO-P is a medical device that received FDA 510(k) clearance on 2008-02-11. The listed applicant is Synthes Spine Co.Lp. The 510(k) number is K072981.
When did SYNTHES ZERO-P receive FDA 510(k) clearance?
SYNTHES ZERO-P received FDA 510(k) clearance on 2008-02-11, under 510(k) number K072981.
Who is the listed applicant for SYNTHES ZERO-P?
The FDA 510(k) record lists Synthes Spine Co.Lp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNTHES ZERO-P?
The FDA product code for SYNTHES ZERO-P is OVE.
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 Synthes Spine Co.Lp 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: OVE)
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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