Atlas FDA

CEMENT EXTRACTOR DRILL

FDA 510(k) clearance K770204 · decided 1977-02-08

Clearance details

K-number
K770204
Device name
CEMENT EXTRACTOR DRILL
Applicant
Depuy, Inc.
Decision
Substantially Equivalent
Date received
1977-01-31
Decision date
1977-02-08
Days to decision
8 days
Clearance type
Traditional
Product code
HXY
Device class
1
Regulation number
888.4540
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
BENDEREV DRILL GUIDE (K923776)Neimark Labs, Inc.1992-11-06
MITEK DRILL GUIDE (K892904)Mitek Surgical Products, Inc.1989-09-28
BONE SUTURE FIXATION DEVICE (K880264)Orthopedic Systems, Inc.1988-03-23
TELOS DISTAL TARGETING DEVICE (K880381)Austin Assoc.1988-03-15
HASTING FINGER FIXATOR INSTRUMENTS (K880046)Buckman Co., Inc.1988-02-16
ANDREWS REMOTE CHUCK DRILL (K831043)Orthopedic Systems, Inc.1983-04-28

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