Atlas FDA

DRIVER-BENDER-EXTRACTOR, BONE PIN

FDA 510(k) clearance K870668 · decided 1987-03-09

Clearance details

K-number
K870668
Device name
DRIVER-BENDER-EXTRACTOR, BONE PIN
Applicant
Military Engineering, Inc.
Decision
Substantially Equivalent
Date received
1987-02-19
Decision date
1987-03-09
Days to decision
18 days
Clearance type
Traditional
Product code
HXW
Device class
1
Regulation number
888.4540
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Plymouth, IN, 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
ACROMED BONE PLATE BENDER (K872949)Buckman Co., Inc.1987-10-15
RD 140 SURGICAL BENDER (K870084)Terray Manufacturing, Inc.1987-01-28

Recalls involving this device

No recalls on record reference this clearance.