Atlas FDA

KNEE INSTRUMENTATION, CONDYLAR

FDA 510(k) clearance K781091 · decided 1978-07-17

Clearance details

K-number
K781091
Device name
KNEE INSTRUMENTATION, CONDYLAR
Applicant
Biomet, Inc.
Decision
Substantially Equivalent
Date received
1978-07-03
Decision date
1978-07-17
Days to decision
14 days
Clearance type
Traditional
Product code
HWT
Device class
1
Regulation number
888.4800
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Walker, MI, 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
WORRELL TRIAL PATELLA (K771709)Depuy, Inc.1977-10-06
WORRELL PATELLA TEMPLATE (K771710)Depuy, Inc.1977-10-06

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
C2A-TAPER ACETABULAR HIP SYSTEM (P050009/S009)Biomet, Inc.2011-02-11
C2A-TAPER ACETABULAR SYSTEM (P050009/S004)Biomet, Inc.2009-04-17
C2A TAPER ACETABULAR SYSTEM (P050009/S007)Biomet, Inc.2009-03-13
C2-A TAPER ACETABULAR SYSTEM (P050009/S005)Biomet, Inc.2007-11-30
C2A-TAPER ACETABULAR SYSTEM (P050009/S002)Biomet, Inc.2006-06-16
C2A-TAPER ACETABULAR SYSTEM (P050009/S001)Biomet, Inc.2006-02-01
C2 A-TAPER ACETABULAR SYSTEM (P050009)Biomet, Inc.2005-12-16