Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Von Zeppelin GmbH · Predicate Candidate Screening

5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

146 daysmedian FDA review time
364 days90th percentile
5clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K013091ZMM 2000 ZEPPELIN MILLENNIUM MOTORDRILL SYSTEMVon Zeppelin GmbH2002-01-251300
K954658PERNECZKY CLIP APPLIER/REMOVERVon Zeppelin GmbH1996-10-083640
K903151INTERVERTEBRAL DISC RONGEURVon Zeppelin GmbH1990-12-111460
K901312PERNECZKY ANEURYSM CLIPVon Zeppelin GmbH1990-08-171500
K901313INSTRUMENTS FOR NEUROLOGICAL SURGERYVon Zeppelin GmbH1990-07-231250

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda