Atlas FDA

WORRELL PATELLA TEMPLATE

FDA 510(k) clearance K771710 · decided 1977-10-06

Clearance details

K-number
K771710
Device name
WORRELL PATELLA TEMPLATE
Applicant
Depuy, Inc.
Decision
Substantially Equivalent
Date received
1977-09-12
Decision date
1977-10-06
Days to decision
24 days
Clearance type
Traditional
Product code
HWT
Device class
1
Regulation number
888.4800
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
ORTHOPLAN (K974406)Ortho-Graphics, Inc.1998-02-18
ORTHODOC PREOPERATIVE PLANNER MODEL 500 (K960685)Integrated Surgical Systems, Inc.1997-01-17
KRONNER SPHERICAL CUTTERS (K894228)Kronner Medical1990-07-23
SCHULTZ PHALANGEAL COMP TRIAL/METACARPAL COMP TRIA (K870843)Warsaw Orthopedic, Inc.1987-05-27
ARTHROSCOPIC MENISCAL SUTURE SYSTEM (K871323)Orthopedic Systems, Inc.1987-05-01
3M OSTEOTOMY GUIDE (K830360)3M Company1983-03-01
MOLDED POLYSULFONE TRIAL PROSTHESIS (K811205)Shannon Group1981-05-21
KNEE INSTRUMENTATION, CONDYLAR (K781091)Biomet, Inc.1978-07-17
WORRELL TRIAL PATELLA (K771709)Depuy, Inc.1977-10-06

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