Atlas FDA

TOTAL SPINAL CORRECTION

FDA 510(k) clearance K760649 · decided 1976-10-05

Clearance details

K-number
K760649
Device name
TOTAL SPINAL CORRECTION
Applicant
Depuy, Inc.
Decision
Substantially Equivalent
Date received
1976-09-15
Decision date
1976-10-05
Days to decision
20 days
Clearance type
Traditional
Product code
JDN
Device class
2
Regulation number
888.3060
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
CANNULATED FEMORAL NAIL (K954856)Synthes (Usa)1996-03-08
SLOT STAPLES AND ADAPTOR FOR ZIELKE SPINAL FIXATIO (K897141)Stuart1990-06-21
BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEM (K894184)Biedermann Motech GmbH1990-04-25
UNIVERSAL INSTRUMENTATION(CD) FOR SPINAL SURGERY (K872715)Roseburg SA1987-12-07
NEW C-D SYSTEM FOR SPINAL SURGERY (K873977)Sofamor Co.1987-12-07

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
ATTUNE™ Revision Rotating Platform (RP) Knee System (P830055/S346)Depuy, Inc.2025-12-18
LCS Total Knee System (P830055/S355)Depuy, Inc.2025-12-15
LCS® Total Knee System (P830055/S354)Depuy, Inc.2025-12-11
LCS® Total Knee System (P830055/S353)Depuy, Inc.2025-12-09
LCS® Total Knee System (P830055/S352)Depuy, Inc.2025-11-26
LCS® Total Knee System (P830055/S350)Depuy, Inc.2025-09-26
LCS® Total Knee System (P830055/S349)Depuy, Inc.2025-09-09
LCS Total Knee System (P830055/S348)Depuy, Inc.2025-08-29