ClearanceBrief
510(k) K970378 ยท KIJ Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment

STRYKER 2115 REPLACEMENT BATTERY (2115)

ApplicantImplant Resource, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Apr 30, 1997
ReceivedJan 31, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970378

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.