Atlas FDA

KeriFlex® MCP and PIP Finger Joint Prostheses

FDA 510(k) clearance K211385 · decided 2022-07-27

Clearance details

K-number
K211385
Device name
KeriFlex® MCP and PIP Finger Joint Prostheses
Applicant
Keri Medical SA
Decision
Substantially Equivalent
Date received
2021-05-04
Decision date
2022-07-27
Days to decision
449 days
Clearance type
Traditional
Product code
KYJ
Device class
2
Regulation number
888.3230
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Geneva, CH
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
Ascension Silicone MCP; Ascension Silicone PIP (K233670)Ascension Orthopedics, Inc.2023-12-14
BRM Digitalis Spacer (K220142)Brm Extremities Srl2023-04-04
OSTEOTEC SILICONE FINGER IMPLANT (K140453)Osteotec, Ltd.2015-04-17
MODIFICATION TO DEPUY NEUFLEX PIP FINGER (K083107)DePuy Orthopaedics, Inc.2009-02-09
ASCENSION SILICONE PIP (K082231)Ascension Orthopedics, Inc.2009-01-12
ASCENSION SILLICONE MCP (K022892)Ascension Orthopedics, Inc.2002-11-25
FINGER JOINT PROSTHESIS (K013629)Avanta Orthopaedics, Inc.2002-01-25
DEPUY NEUFLEX PIP FINGER (K001922)Depuy, Inc.2000-08-29
DEPUY DUPONT ORTHOPAEDICS FINGER JOINT PROSTHESIS (K970544)Depuy, Inc.1997-09-12
SUTTER PROXIMAL INTERPHALANGEAL JOINT (K931588)Sutter Corp.1994-03-10
SUTTER FINGER JOINT PROSTHESIS (K870200)Sutter Biomedical, Inc.1987-10-09
MARNE M.T.P.J. ORTHOPEDIC IMPLANT (K781380)Farah , Ltd.1979-02-21

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
TOUCH® CMC 1 Prosthesis (P240020/S003)Keri Medical SA2025-12-17
TOUCH® CMC 1 Prosthesis (P240020/S001)Keri Medical SA2025-09-05
TOUCH® CMC 1 Prosthesis (P240020/S002)Keri Medical SA2025-09-05
TOUCH® CMC 1 Prosthesis (P240020)Keri Medical SA2025-07-10