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Baumer Femoral Head

by Baumer, S.A Brazil 510(k)

510(k) K001571 Product code JDI

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK001571 Date4 Aug 2000ClearedStatusActive

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — FDA 510(k) Active

Recalls: none on record (FDA, checked 22 Oct 2026)

Specification

510(k) · synced 22 Oct 2026

510(k) Number
FDA Product Code
JDI
Device Class
Class II
Regulation
21 CFR Part 888.3350
Advisory Committee
Orthopedic
FDA Decision
SESE Substantially Equivalent

Other devices from Baumer, S.A

Properties & raw data

Show properties, registry sources and raw records

Sources (1)

  • FDA 510(k) K001571 24 fields · synced 22 Oct 2026