Biolox Delta Ceramic Femoral Head

510(k) K071535

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

3 closed

Documents

FDA record

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK071535	Date19 Nov 2007Cleared	StatusActive

3 recalls · FDA

- Terminated Z-0336-2020 FDA Class II initiated 10 Oct 2019
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
- Terminated Z-1134-2015 FDA Class II initiated 17 Dec 2014
Potential compromise of the inner sterile tray. If a compromised tray is detected, a delay in surgery may result. If undetected breach in both the inner and outer trays were to occur, and there is contamination present, a periprosthetic infection is possible, which could lead to revision.
- Terminated Z-0211-2013 FDA Class II initiated 4 Sep 2012
Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info

1 jurisdiction

United States — FDA 510(k) Active

510(k)