Product code JDN— Orthopedic

FDA has cleared 6 devices under product code JDN between 1976 and 1996, filed by 6 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

• 19961 clearance
• 19902 clearances
• 19872 clearances
• 19761 clearance

• Synthes (Usa)1 clearance
• Stuart1 clearance
• Sofamor Co.1 clearance
• Roseburg SA1 clearance
• Depuy, Inc.1 clearance
• Biedermann Motech GmbH1 clearance

• K954856 — CANNULATED FEMORAL NAILSynthes (Usa)·1996-03-08
• K897141 — SLOT STAPLES AND ADAPTOR FOR ZIELKE SPINAL FIXATIOStuart·1990-06-21
• K894184 — BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEMBiedermann Motech GmbH·1990-04-25
• K872715 — UNIVERSAL INSTRUMENTATION(CD) FOR SPINAL SURGERYRoseburg SA·1987-12-07
• K873977 — NEW C-D SYSTEM FOR SPINAL SURGERYSofamor Co.·1987-12-07
• K760649 — TOTAL SPINAL CORRECTIONDepuy, Inc.·1976-10-05