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)

SYNTHES ZERO-P

K-Number: K072981 · 2008-02-11

Decision Date2008-02-11
Product CodeOVE
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SYNTHES ZERO-P is the device name listed in this FDA 510(k) record. The listed applicant is Synthes Spine Co.Lp. It received FDA 510(k) clearance on 2008-02-11 under 510(k) number K072981. The device is classified under product code OVE. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 18 devices →

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.

↑