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

Memometal Technologies — Predicate Candidate Screening

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

108 daysmedian FDA review time
249 days90th percentile
10clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K112197MEMOMETAL INTRA-MEDULLARY BONE FASTENERMemometal Technologies2011-11-171080
K101930MEMOMETAL NAVIS BONE PLATING SYSTEMMemometal Technologies2011-03-152490
K102072MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE)Memometal Technologies2010-11-031030
K093820SUBFIX ARTHROEREISIS IMPLANT, MODELS SUT0065, SUT0080, SUT00Memometal Technologies2010-05-191560
K083447MEMOMETAL ANCHORAGE BONE PLATE SYSTEM, MODELS PLSS/PLSL, PLPMemometal Technologies2009-02-06770
K071941MEMOMETAL BONE ANCHORSMemometal Technologies2007-12-041440
K070598MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MODELS SMART TOE / Memometal Technologies2007-07-261460
K070039MEMOMETAL FIXOS SCREWSMemometal Technologies2007-03-21770
K070033MEMOMETAL VARISATION, MODELS AV26-08, AV26-10, AV90-08 AND AMemometal Technologies2007-03-19750
K070031MEMOMETAL MEMORY STAPLESMemometal Technologies2007-03-19750

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